[ CAS No. 394-67-2 ] {[proInfo.proName]}

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Quality Control of [ 394-67-2 ]

COA NMR CNMR HPLC LC-MS

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SDS Specification

Alternatived Products of [ 394-67-2 ]

Product Details of [ 394-67-2 ]

CAS No. :	394-67-2	MDL No. :	MFCD06656128
Formula :	C₉H₆FN	Boiling Point :	No data available
Linear Structure Formula :	-	InChI Key :	VFFQGPWQVYUFLV-UHFFFAOYSA-N
M.W :	147.15	Pubchem ID :	640973
Synonyms :

Calculated chemistry of [ 394-67-2 ] Expand+

Physicochemical Properties

Num. heavy atoms :	11
Num. arom. heavy atoms :	10
Fraction Csp3 :	0.0
Num. rotatable bonds :	0
Num. H-bond acceptors :	2.0
Num. H-bond donors :	0.0
Molar Refractivity :	41.7
TPSA :	12.89 ?2

Pharmacokinetics

GI absorption :	High
BBB permeant :	Yes
P-gp substrate :	No
CYP1A2 inhibitor :	Yes
CYP2C19 inhibitor :	No
CYP2C9 inhibitor :	No
CYP2D6 inhibitor :	No
CYP3A4 inhibitor :	No
Log Kp (skin permeation) :	-5.64 cm/s

Lipophilicity

Log Po/w (iLOGP) :	1.83
Log Po/w (XLOGP3) :	2.2
Log Po/w (WLOGP) :	2.79
Log Po/w (MLOGP) :	2.0
Log Po/w (SILICOS-IT) :	2.91
Consensus Log Po/w :	2.35

Druglikeness

Lipinski :	0.0
Ghose :	None
Veber :	0.0
Egan :	0.0
Muegge :	2.0
Bioavailability Score :	0.55

Water Solubility

Log S (ESOL) :	-2.81
Solubility :	0.227 mg/ml ; 0.00155 mol/l
Class :	Soluble
Log S (Ali) :	-2.1
Solubility :	1.16 mg/ml ; 0.00786 mol/l
Class :	Soluble
Log S (SILICOS-IT) :	-3.96
Solubility :	0.0162 mg/ml ; 0.00011 mol/l
Class :	Soluble

Medicinal Chemistry

PAINS :	0.0 alert
Brenk :	0.0 alert
Leadlikeness :	1.0
Synthetic accessibility :	1.37

Safety of [ 394-67-2 ]

Signal Word:	Warning	Class:
Precautionary Statements:	P261-P305+P351+P338	UN#:
Hazard Statements:	H302-H315-H319-H335	Packing Group:
GHS Pictogram:

Application In Synthesis of [ 394-67-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

Upstream synthesis route of [ 394-67-2 ]
Downstream synthetic route of [ 394-67-2 ]

[ 394-67-2 ] Synthesis Path-Upstream 1~4

1
[ 1532-97-4 ]
[ 394-67-2 ]

Yield	Reaction Conditions	Operation in experiment
60%	Stage #1: With n-butyllithium In tetrahydrofuran at -65℃; for 0.5 h; Stage #2: With N-fluorobis(benzenesulfon)imide In tetrahydrofuran at -65℃; for 2 h;	To a solution of n-butyl lithium (133 mL, 332.5 mmol, 2.5 M in THF) in 760 mL THF was added a solution of 4-bromoisoquinoline 24a (20 g, 96.6 mmol) in 144 mL THF dropwise at -65° C. and the resulting mixture was stirred at this temperature for another 30 mm after the completion of addition. A solution of N-fluorobenzenesulfonimide (66.68 g, 211.7 mmol) in 216 mL THF was added at -65° C. in 1 h dropwisely. After being stirred for another 1 h at this temperature, the reaction mixture was warmed to room temperature slowly with stirring, after the reaction is over, 300 mL saturated aq. NH₄Cl was added slowly, extracted with EtOAc (300 mL*3). The combined organic layers were washed with 300 mL brine, dried over anhydrous Na₂SO₄ and concentrated. The crude product was purified by silica gel column chromatography (0-100percent EtOAc/PE) to give 4-fluoroisoquinoline 24b (8.5 g, red oil, yield: 60percent).

Reference： [1] Journal of the American Chemical Society, 2014, vol. 136, # 10, p. 3792 - 3795
[2] Patent: US2017/37050, 2017, A1, . Location in patent: Paragraph 0301; 0302
[3] Patent: US2007/179127, 2007, A1, . Location in patent: Page/Page column 47-48
[4] Patent: US2009/48223, 2009, A1, . Location in patent: Page/Page column 101
[5] Patent: US2010/93789, 2010, A1, . Location in patent: Page/Page column 46

2
[ 23687-25-4 ]
[ 394-67-2 ]

Reference： [1] Angewandte Chemie - International Edition, 2016, vol. 55, # 39, p. 11907 - 11911[2] Angew. Chem., 2016, vol. 128, p. 12086 - 12090,5
[3] Journal of the American Chemical Society, 2017, vol. 139, # 24, p. 8267 - 8276
[4] Patent: EP1074545, 2001, A1,

3
[ 491-30-5 ]
[ 119-65-3 ]
[ 394-67-2 ]

Reference： [1] Patent: JP2018/70562, 2018, A,
[2] Patent: JP2018/70562, 2018, A,
[3] Patent: JP2018/70562, 2018, A,
[4] Patent: JP2018/70562, 2018, A,

4
[ 491-30-5 ]
[ 394-67-2 ]

Reference： [1] Patent: CN108558758, 2018, A,

[ 394-67-2 ] Synthesis Path-Downstream 1~18

1
[ 394-67-2 ]
[ 906820-09-5 ]

Reference： [1]Heterocycles,2011,vol. 83,p. 1771 - 1781
[2]Patent: WO2006/90783,2006,A1 .Location in patent: Page/Page column 8

2
[ 394-67-2 ]
[ 1334294-10-8 ]
[ 906820-08-4 ]

Reference： [1]Patent: WO2006/90783,2006,A1 .Location in patent: Page/Page column 7-8
[2]Heterocycles,2011,vol. 83,p. 1771 - 1781
[3]Heterocycles,2011,vol. 83,p. 1771 - 1781

3
[ 23687-25-4 ]
[ 394-67-2 ]

Yield	Reaction Conditions	Operation in experiment
		From 4-aminoisoquinoline (20.0 g), 4-fluoroisoquinoline (9.61 g) was obtained following J. Am. Chem. Soc., 73, 683 (1951).

Reference： [1]Angewandte Chemie - International Edition,2016,vol. 55,p. 11907 - 11911
Angew. Chem.,2016,vol. 128,p. 12086 - 12090,5
[2]Journal of the American Chemical Society,2017,vol. 139,p. 8267 - 8276
[3]Patent: EP1074545,2001,A1

4
[ 394-67-2 ]
[ 928664-13-5 ]

Yield	Reaction Conditions	Operation in experiment
		Reference Example 2 4-Fluoro-5-nitroisoquinoline <strong>[394-67-2]4-Fluoroisoquinoline</strong> (3.6 g) obtained in Reference Example 1 was dissolved in concentrated sulfuric acid (20 ml), and the solution was added dropwise with a solution of potassium nitrate (3.25 g, Wako Pure Chemical Industries) in concentrated sulfuric acid (28 ml) under cooling at -5° C. so that the temperature of the reaction mixture should not exceed 5° C. The reaction mixture was stirred at 0° C. for 1 hour, poured into ice water, neutralized with 28percent aqueous ammonia (pH 8), and extracted 3 times with ethyl acetate (150 ml for each time). The combined organic layer was washed with saturated aqueous sodium hydrogencarbonate (300 ml), and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography (n-hexane:ethyl acetate=3:1) to obtain the title compound (2.2 g).
	With sulfuric acid; potassium nitrate; In water; at -5 - 0℃; for 1h;	<strong>[394-67-2]4-Fluoroisoquinoline</strong> (3.6 g) obtained in Reference Example 1 was dissolved in concentrated sulfuric acid (20 ml), and the solution was added dropwise with a solution of potassium nitrate (3.25 g, Wako Pure Chemical Industries) in concentrated sulfuric acid (28 ml) under cooling at -5° C. so that the temperature of the reaction mixture should not exceed 5° C. The reaction mixture was stirred at 0° C. for 1 hour, poured into ice water, neutralized with 28percent aqueous ammonia (pH 8), and extracted 3 times with ethyl acetate (150 ml for each time). The combined organic layer was washed with saturated aqueous sodium hydrogencarbonate (300 ml), and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography (n-hexane:ethyl acetate=3:1) to obtain the title compound (2.2 g).
		Reference Example 2; 4-Fluoro-5-nitroisoquinoline; <strong>[394-67-2]4-Fluoroisoquinoline</strong> (3.6 g) obtained in Reference Example 1 was dissolved in concentrated sulfuric acid (20 ml), and the solution was added dropwise with a solution of potassium nitrate (3.25 g, Wako Pure Chemical Industries) in concentrated sulfuric acid (28 ml) under cooling at -5° C. so that the temperature of the reaction mixture should not exceed 5° C. The reaction mixture was stirred at 0° C. for 1 hour, poured into ice water, neutralized with 28percent aqueous ammonia (pH 8), and extracted 3 times with ethyl acetate (150 ml for each time). The combined organic layer was washed with saturated aqueous sodium hydrogencarbonate (300 ml), and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography (n-hexane:ethyl acetate=3:1) to obtain the title compound (2.2 g).

23 g

With sulfuric acid; nitric acid; at 0 - 20℃; for 3h;

Add 50 ml of sulfuric acid to the reaction flask and cool to T=0 °C.<strong>[394-67-2]4-Fluoroisoquinoline</strong> (29 g, 0.2 mmol) was added in portions.Nitric acid (1.3 eq) was added dropwise and allowed to react to room temperature for 3 h.Add the reaction solution to the ice cube, NaOHaq. Adjust pH=11,After suction filtration, the filter residue was washed with water to obtain 23 g of product.Go directly to the next step.

Reference： [1]Patent: US2007/179127,2007,A1 .Location in patent: Page/Page column 48
[2]Patent: US2009/48223,2009,A1 .Location in patent: Page/Page column 101
[3]Patent: US2010/93789,2010,A1 .Location in patent: Page/Page column 46
[4]Patent: CN108558758,2018,A .Location in patent: Paragraph 0057; 0058

5
[ 1532-97-4 ]
[ 394-67-2 ]

Yield	Reaction Conditions	Operation in experiment
60%		To a solution of n-butyl lithium (133 mL, 332.5 mmol, 2.5 M in THF) in 760 mL THF was added a solution of 4-bromoisoquinoline 24a (20 g, 96.6 mmol) in 144 mL THF dropwise at -65° C. and the resulting mixture was stirred at this temperature for another 30 mm after the completion of addition. A solution of N-fluorobenzenesulfonimide (66.68 g, 211.7 mmol) in 216 mL THF was added at -65° C. in 1 h dropwisely. After being stirred for another 1 h at this temperature, the reaction mixture was warmed to room temperature slowly with stirring, after the reaction is over, 300 mL saturated aq. NH4Cl was added slowly, extracted with EtOAc (300 mL*3). The combined organic layers were washed with 300 mL brine, dried over anhydrous Na2SO4 and concentrated. The crude product was purified by silica gel column chromatography (0-100percent EtOAc/PE) to give 4-fluoroisoquinoline 24b (8.5 g, red oil, yield: 60percent).
		Reference Example 1 4-Fluoroisoquinoline A solution of n-butyllithium in n-hexane (1.58 M, 60.1 ml, Kanto Chemicals) was added with tetrahydrofuran (345 ml), and the mixture was sufficiently cooled on a dry ice-acetone bath. The mixture was added dropwise with a solution of 4-bromoisoquinoline (9.0 g, Tokyo Kasei Kogyo) in tetrahydrofuran (65 ml) over 1 hour so that the temperature of the reaction mixture should not exceed -65° C. The mixture was stirred at the same temperature for 30 minutes, and then added dropwise with a solution of N-fluorobenzenesulfonimide (30 g, Tokyo Kasei Kogyo) in tetrahydrofuran (100 ml) over 1 hour so that the temperature of the reaction mixture should not exceed -65° C. Subsequently, the mixture was stirred at the same temperature for 1 hour, then the cooling bath was removed, and the mixture was gradually warmed to room temperature. The reaction mixture was added with saturated aqueous sodium hydrogencarbonate (300 ml) and ethyl acetate (300 ml), and stirred at room temperature for 12 hours. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate 3 times (200 ml for each time). The combined organic layer was washed with saturated brine (500 ml), and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, the residue was added with chloroform (250 ml), and the insoluble matters were removed by filtration. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography (n-hexane:ethyl acetate=5:1) to obtain the title compound (3.6 g). MS (m/z): 148 (MH+) 1H-NMR (CDCl3) delta (ppm): 7.26-7.71 (1H, m), 7.75-7.82 (1H, m), 8.03 (1H, dd, J=1.2 Hz, J=8.4 Hz), 8.10 (1H, d, J=8.4 Hz), 8.38 (1H, s), 9.08 (1H, s)
		A solution of n-butyllithium in n-hexane (1.58 M, 60.1 ml, Kanto Chemicals) was added with tetrahydrofuran (345 ml), and the mixture was sufficiently cooled on a dry ice-acetone bath. The mixture was added dropwise with a solution of 4-bromoisoquinoline (9.0 g, Tokyo Kasei Kogyo) in tetrahydrofuran (65 ml) over 1 hour so that the temperature of the reaction mixture should not exceed -65° C. The mixture was stirred at the same temperature for 30 minutes, and then added dropwise with a solution of N-fluorobenzenesulfonimide (30 g, Tokyo Kasei Kogyo) in tetrahydrofuran (100 ml) over 1 hour so that the temperature of the reaction mixture should not exceed -65° C. Subsequently, the mixture was stirred at the same temperature for 1 hour, then the cooling bath was removed, and the mixture was gradually warmed to room temperature. The reaction mixture was added with saturated aqueous sodium hydrogencarbonate (300 ml) and ethyl acetate (300 ml), and stirred at room temperature for 12 hours. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate 3 times (200 ml for each time). The combined organic layer was washed with saturated brine (500 ml), and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, the residue was added with chloroform (250 ml), and the insoluble solids were removed by filtration. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography (n-hexane:ethyl acetate=5:1) to obtain the title compound (3.6 g).MS (m/z): 148 (MH+)1H-NMR (CDCl3) delta (ppm): 7.26-7.71 (1H, m), 7.75-7.82 (1H, m), 8.03 (1H, dd, J=1.2 Hz, J=8.4 Hz), 8.10 (1H, d, J=8.4 Hz), 8.38 (1H, s), 9.08 (1H, s)

Reference Example 1; 4-Fluoroisoquinoline; A solution of n-butyllithium in n-hexane (1.58 M, 60.1 ml, Kanto Chemicals) was added with tetrahydrofuran (345 ml), and the mixture was sufficiently cooled on a dry ice-acetone bath. The mixture was added dropwise with a solution of 4-bromoisoquinoline (9.0 g, Tokyo Kasei Kogyo) in tetrahydrofuran (65 ml) over 1 hour so that the temperature of the reaction mixture should not exceed -65° C. The mixture was stirred at the same temperature for 30 minutes, and then added dropwise with a solution of N-fluorobenzenesulfonimide (30 g, Tokyo Kasei Kogyo) in tetrahydrofuran (100 ml) over 1 hour so that the temperature of the reaction mixture should not exceed -65° C. Subsequently, the mixture was stirred at the same temperature for 1 hour, then the cooling bath was removed, and the mixture was gradually warmed to room temperature. The reaction mixture was added with saturated aqueous sodium hydrogencarbonate (300 ml) and ethyl acetate (300 ml), and stirred at room temperature for 12 hours. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate 3 times (200 ml for each time). The combined organic layer was washed with saturated brine (500 ml), and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, the residue was added with chloroform (250 ml), and the insoluble solids were removed by filtration. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography (n-hexane:ethyl acetate=5:1) to obtain the title compound (3.6 g).MS (m/z): 148 (MH+)1H-NMR (CDCl3) delta (ppm): 7.26-7.71 (1H, m), 7.75-7.82 (1H, m), 8.03 (1H, dd, J=1.2 Hz, J=8.4 Hz), 8.10 (1H, d, J=8.4 Hz), 8.38 (1H, s), 9.08 (1H, s)

Reference： [1]Journal of the American Chemical Society,2014,vol. 136,p. 3792 - 3795
[2]Patent: US2017/37050,2017,A1 .Location in patent: Paragraph 0301; 0302
[3]Patent: US2007/179127,2007,A1 .Location in patent: Page/Page column 47-48
[4]Patent: US2009/48223,2009,A1 .Location in patent: Page/Page column 101
[5]Patent: US2010/93789,2010,A1 .Location in patent: Page/Page column 46

6
[ 394-67-2 ]
[ 223644-12-0 ]

Reference： [1]Heterocycles,2011,vol. 83,p. 1771 - 1781
[2]Heterocycles,2011,vol. 83,p. 1771 - 1781

7
[ 394-67-2 ]
C₁₂H₁₁FN₂O₂S [ No CAS ]
C₁₃H₁₅FN₂O₅S₂ [ No CAS ]

Reference： [1]Heterocycles,2011,vol. 83,p. 1771 - 1781
[2]Heterocycles,2011,vol. 83,p. 1771 - 1781

8
[ 394-67-2 ]
(S)-4-fluoro-N-[1-(3-hydroxypropylamino)propan-2-yl]isoquinoline-5-sulfonamide oxalate [ No CAS ]

Reference： [1]Heterocycles,2011,vol. 83,p. 1771 - 1781
[2]Heterocycles,2011,vol. 83,p. 1771 - 1781

9
[ 394-67-2 ]
[ 223644-02-8 ]

Reference： [1]Heterocycles,2011,vol. 83,p. 1771 - 1781
[2]Heterocycles,2011,vol. 83,p. 1771 - 1781

10
[ 394-67-2 ]
[ 906820-10-8 ]
[ 1334294-09-5 ]

Yield	Reaction Conditions	Operation in experiment
	With phosphotungstic acid; sulfuric acid; sulfur trioxide; at 30℃; for 3h;	<strong>[394-67-2]4-fluoroisoquinoline</strong> (10 mmol, 1.47 g), 98percent by weight of concentrated sulfuric acid (22 mmol, 2.2 eq), and three were added to the reaction flask.Sulfur oxide (86mmol, 8.6eq), additive (0.3g, ~20percent wt) reacted at 30 ° C, HPLC detection of <strong>[394-67-2]4-fluoroisoquinoline</strong> no longerDuring the conversion, the starting material <strong>[394-67-2]4-fluoroisoquinoline</strong> (Compound A compound), the target product <strong>[394-67-2]4-fluoroisoquinoline</strong>-5-sulfonic acid (Compound B compound) and its by-product <strong>[394-67-2]4-fluoroisoquinoline</strong>-8 were counted in the reaction solution. The area percentage of the -sulfonic acid (compound of formula C)

Reference： [1]Heterocycles,2011,vol. 83,p. 1771 - 1781
[2]Heterocycles,2011,vol. 83,p. 1771 - 1781
[3]Patent: CN108912046,2018,A .Location in patent: Paragraph 0030; 0031; 0032; 0033; 0034; 0035-0049

11
[ 394-67-2 ]
[ 194032-33-2 ]
C₉H₅ClFNO₂S [ No CAS ]

Reference： [1]Heterocycles,2011,vol. 83,p. 1771 - 1781

12
[ 394-67-2 ]
[ 1008-32-8 ]

Reference： [1]Organic Letters,2013,vol. 15,p. 792 - 795

13
[ 394-67-2 ]
[ 1421517-86-3 ]

Reference： [1]Organic Letters,2013,vol. 15,p. 792 - 795

14
[ 491-30-5 ]
[ 119-65-3 ]
[ 394-67-2 ]

Reference： [1]Patent: JP2018/70562,2018,A
[2]Patent: JP2018/70562,2018,A
[3]Patent: JP2018/70562,2018,A
[4]Patent: JP2018/70562,2018,A

15
C₁₀H₁₀FNO₂ [ No CAS ]
[ 119-65-3 ]
[ 394-67-2 ]

Reference： [1]Patent: JP2018/70562,2018,A
[2]Patent: JP2018/70562,2018,A
[3]Patent: JP2018/70562,2018,A

16
4-fluoroisoquinolin-1(2H)-one [ No CAS ]
[ 119-65-3 ]
[ 394-67-2 ]

Reference： [1]Patent: JP2018/70562,2018,A

17
1-chloro-4-fluoroisoquinoline [ No CAS ]
[ 119-65-3 ]
[ 394-67-2 ]

Yield	Reaction Conditions	Operation in experiment
	With palladium 10% on activated carbon; hydrogen; In ethanol; at 20℃; under 760.051 Torr;	1-chloro-4-fluoroisoquinoline (9a) obtained by the method of Example 3(55 mg) in ethanol (2 mL)10percent Pd charcoal (26 mg; containing 54percent moisture) was added,Under 1 atm hydrogen atmosphere at room temperature until reductive cracking is complete (5 to 15 h)Followed by stirring. The catalyst was removed by filtration, and the filtrate was concentrated under reduced pressure.The residue was dissolved in ethyl acetate-water to remove the aqueous layer, the organic layer was washed with 20percent brine, and dried over anhydrous magnesium sulfate.The solvent was distilled off under reduced pressure to give 4-fluoroisoquinoline (1)And isoquinoline (33 mg) as a colorless oil.

Reference： [1]Patent: JP2018/70562,2018,A .Location in patent: Sheet 0054; 0056

18
[ 491-30-5 ]
[ 394-67-2 ]

Reference： [1]Patent: CN108558758,2018,A

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Ghs Precautionary Statements

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Code	Phrase
P101	If medical advice is needed,have product container or label at hand.
P102	Keep out of reach of children.
P103	Read label before use
Prevention
Code	Phrase
P201	Obtain special instructions before use.
P202	Do not handle until all safety precautions have been read and understood.
P210	Keep away from heat/sparks/open flames/hot surfaces. - No smoking.
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P220	Keep/Store away from clothing/combustible materials.
P221	Take any precaution to avoid mixing with combustibles
P222	Do not allow contact with air.
P223	Keep away from any possible contact with water, because of violent reaction and possible flash fire.
P230	Keep wetted
P231	Handle under inert gas.
P232	Protect from moisture.
P233	Keep container tightly closed.
P234	Keep only in original container.
P235	Keep cool
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P242	Use only non-sparking tools.
P243	Take precautionary measures against static discharge.
P244	Keep reduction valves free from grease and oil.
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P251	Pressurized container: Do not pierce or burn, even after use.
P260	Do not breathe dust/fume/gas/mist/vapours/spray.
P261	Avoid breathing dust/fume/gas/mist/vapours/spray.
P262	Do not get in eyes, on skin, or on clothing.
P263	Avoid contact during pregnancy/while nursing.
P264	Wash hands thoroughly after handling.
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P270	Do not eat, drink or smoke when using this product.
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P273	Avoid release to the environment.
P280	Wear protective gloves/protective clothing/eye protection/face protection.
P281	Use personal protective equipment as required.
P282	Wear cold insulating gloves/face shield/eye protection.
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P284	Wear respiratory protection.
P285	In case of inadequate ventilation wear respiratory protection.
P231 + P232	Handle under inert gas. Protect from moisture.
P235 + P410	Keep cool. Protect from sunlight.
Response
Code	Phrase
P301	IF SWALLOWED:
P304	IF INHALED:
P305	IF IN EYES:
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P308	IF exposed or concerned:
P309	IF exposed or if you feel unwell:
P310	Immediately call a POISON CENTER or doctor/physician.
P311	Call a POISON CENTER or doctor/physician.
P312	Call a POISON CENTER or doctor/physician if you feel unwell.
P313	Get medical advice/attention.
P314	Get medical advice/attention if you feel unwell.
P315	Get immediate medical advice/attention.
P320
P302 + P352	IF ON SKIN: wash with plenty of soap and water.
P321
P322
P330	Rinse mouth.
P331	Do NOT induce vomiting.
P332	IF SKIN irritation occurs:
P333	If skin irritation or rash occurs:
P334	Immerse in cool water/wrap n wet bandages.
P335	Brush off loose particles from skin.
P336	Thaw frosted parts with lukewarm water. Do not rub affected area.
P337	If eye irritation persists:
P338	Remove contact lenses, if present and easy to do. Continue rinsing.
P340	Remove victim to fresh air and keep at rest in a position comfortable for breathing.
P341	If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing.
P342	If experiencing respiratory symptoms:
P350	Gently wash with plenty of soap and water.
P351	Rinse cautiously with water for several minutes.
P352	Wash with plenty of soap and water.
P353	Rinse skin with water/shower.
P360	Rinse immediately contaminated clothing and skin with plenty of water before removing clothes.
P361	Remove/Take off immediately all contaminated clothing.
P362	Take off contaminated clothing and wash before reuse.
P363	Wash contaminated clothing before reuse.
P370	In case of fire:
P371	In case of major fire and large quantities:
P372	Explosion risk in case of fire.
P373	DO NOT fight fire when fire reaches explosives.
P374	Fight fire with normal precautions from a reasonable distance.
P376	Stop leak if safe to do so. Oxidising gases (section 2.4) 1
P377	Leaking gas fire: Do not extinguish, unless leak can be stopped safely.
P378
P380	Evacuate area.
P381	Eliminate all ignition sources if safe to do so.
P390	Absorb spillage to prevent material damage.
P391	Collect spillage. Hazardous to the aquatic environment
P301 + P310	IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.
P301 + P312	IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P301 + P330 + P331	IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
P302 + P334	IF ON SKIN: Immerse in cool water/wrap in wet bandages.
P302 + P350	IF ON SKIN: Gently wash with plenty of soap and water.
P303 + P361 + P353	IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P304 + P312	IF INHALED: Call a POISON CENTER or doctor/physician if you feel unwell.
P304 + P340	IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P304 + P341	IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing.
P305 + P351 + P338	IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P306 + P360	IF ON CLOTHING: Rinse Immediately contaminated CLOTHING and SKIN with plenty of water before removing clothes.
P307 + P311	IF exposed: call a POISON CENTER or doctor/physician.
P308 + P313	IF exposed or concerned: Get medical advice/attention.
P309 + P311	IF exposed or if you feel unwell: call a POISON CENTER or doctor/physician.
P332 + P313	IF SKIN irritation occurs: Get medical advice/attention.
P333 + P313	IF SKIN irritation or rash occurs: Get medical advice/attention.
P335 + P334	Brush off loose particles from skin. Immerse in cool water/wrap in wet bandages.
P337 + P313	IF eye irritation persists: Get medical advice/attention.
P342 + P311	IF experiencing respiratory symptoms: call a POISON CENTER or doctor/physician.
P370 + P376	In case of fire: Stop leak if safe to Do so.
P370 + P378	In case of fire:
P370 + P380	In case of fire: Evacuate area.
P370 + P380 + P375	In case of fire: Evacuate area. Fight fire remotely due to the risk of explosion.
P371 + P380 + P375	In case of major fire and large quantities: Evacuate area. Fight fire remotely due to the risk of explosion.
Storage
Code	Phrase
P401
P402	Store in a dry place.
P403	Store in a well-ventilated place.
P404	Store in a closed container.
P405	Store locked up.
P406	Store in corrosive resistant/ container with a resistant inner liner.
P407	Maintain air gap between stacks/pallets.
P410	Protect from sunlight.
P411
P412	Do not expose to temperatures exceeding 50 oC/ 122 oF.
P413
P420	Store away from other materials.
P422
P402 + P404	Store in a dry place. Store in a closed container.
P403 + P233	Store in a well-ventilated place. Keep container tightly closed.
P403 + P235	Store in a well-ventilated place. Keep cool.
P410 + P403	Protect from sunlight. Store in a well-ventilated place.
P410 + P412	Protect from sunlight. Do not expose to temperatures exceeding 50 oC/122oF.
P411 + P235	Keep cool.
Disposal
Code	Phrase
P501	Dispose of contents/container to ...
P502	Refer to manufacturer/supplier for information on recovery/recycling

Physical hazards
Code	Phrase
H200	Unstable explosive
H201	Explosive; mass explosion hazard
H202	Explosive; severe projection hazard
H203	Explosive; fire, blast or projection hazard
H204	Fire or projection hazard
H205	May mass explode in fire
H220	Extremely flammable gas
H221	Flammable gas
H222	Extremely flammable aerosol
H223	Flammable aerosol
H224	Extremely flammable liquid and vapour
H225	Highly flammable liquid and vapour
H226	Flammable liquid and vapour
H227	Combustible liquid
H228	Flammable solid
H229	Pressurized container: may burst if heated
H230	May react explosively even in the absence of air
H231	May react explosively even in the absence of air at elevated pressure and/or temperature
H240	Heating may cause an explosion
H241	Heating may cause a fire or explosion
H242	Heating may cause a fire
H250	Catches fire spontaneously if exposed to air
H251	Self-heating; may catch fire
H252	Self-heating in large quantities; may catch fire
H260	In contact with water releases flammable gases which may ignite spontaneously
H261	In contact with water releases flammable gas
H270	May cause or intensify fire; oxidizer
H271	May cause fire or explosion; strong oxidizer
H272	May intensify fire; oxidizer
H280	Contains gas under pressure; may explode if heated
H281	Contains refrigerated gas; may cause cryogenic burns or injury
H290	May be corrosive to metals
Health hazards
Code	Phrase
H300	Fatal if swallowed
H301	Toxic if swallowed
H302	Harmful if swallowed
H303	May be harmful if swallowed
H304	May be fatal if swallowed and enters airways
H305	May be harmful if swallowed and enters airways
H310	Fatal in contact with skin
H311	Toxic in contact with skin
H312	Harmful in contact with skin
H313	May be harmful in contact with skin
H314	Causes severe skin burns and eye damage
H315	Causes skin irritation
H316	Causes mild skin irritation
H317	May cause an allergic skin reaction
H318	Causes serious eye damage
H319	Causes serious eye irritation
H320	Causes eye irritation
H330	Fatal if inhaled
H331	Toxic if inhaled
H332	Harmful if inhaled
H333	May be harmful if inhaled
H334	May cause allergy or asthma symptoms or breathing difficulties if inhaled
H335	May cause respiratory irritation
H336	May cause drowsiness or dizziness
H340	May cause genetic defects
H341	Suspected of causing genetic defects
H350	May cause cancer
H351	Suspected of causing cancer
H360	May damage fertility or the unborn child
H361	Suspected of damaging fertility or the unborn child
H361d	Suspected of damaging the unborn child
H362	May cause harm to breast-fed children
H370	Causes damage to organs
H371	May cause damage to organs
H372	Causes damage to organs through prolonged or repeated exposure
H373	May cause damage to organs through prolonged or repeated exposure
Environmental hazards
Code	Phrase
H400	Very toxic to aquatic life
H401	Toxic to aquatic life
H402	Harmful to aquatic life
H410	Very toxic to aquatic life with long-lasting effects
H411	Toxic to aquatic life with long-lasting effects
H412	Harmful to aquatic life with long-lasting effects
H413	May cause long-lasting harmful effects to aquatic life
H420	Harms public health and the environment by destroying ozone in the upper atmosphere

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[ CAS No. 394-67-2 ] {[proInfo.proName]}

Quality Control of [ 394-67-2 ]

Related Doc. of [ 394-67-2 ]

Product Details of [ 394-67-2 ]

Calculated chemistry of [ 394-67-2 ] Expand+

Physicochemical Properties

Pharmacokinetics

Lipophilicity

Druglikeness

Water Solubility

Medicinal Chemistry

Safety of [ 394-67-2 ]

Application In Synthesis of [ 394-67-2 ]

[ 394-67-2 ] Synthesis Path-Upstream 1~4

[ 394-67-2 ] Synthesis Path-Downstream 1~18

Technical Information

Related Functional Groups of [ 394-67-2 ]

Fluorinated Building Blocks

Related Parent Nucleus of [ 394-67-2 ]

Isoquinolines

Precautionary Statements-General

Prevention

Response

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Physical hazards

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Inquiry

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[ 394-67-2 ]

Related Parent Nucleus of
[ 394-67-2 ]