[ CAS No. 6092-54-2 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}

Cat. No.: {[proInfo.prAm]}

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Type	HazMat fee for 500 gram (Estimated)
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Limited Quantity	USD 15-60
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2D 3D

Structure of 6092-54-2 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 6092-54-2 ]

COA NMR CNMR HPLC LC-MS

Related Doc. of [ 6092-54-2 ]

SDS Specification

Alternatived Products of [ 6092-54-2 ]

Product Details of [ 6092-54-2 ]

CAS No. :	6092-54-2	MDL No. :	MFCD00000651
Formula :	C₇H₁₃ClO₂	Boiling Point :	No data available
Linear Structure Formula :	-	InChI Key :	KIWBRXCOTCXSSZ-UHFFFAOYSA-N
M.W :	164.63	Pubchem ID :	22466
Synonyms :

Calculated chemistry of [ 6092-54-2 ] Expand+

Physicochemical Properties

Num. heavy atoms :	10
Num. arom. heavy atoms :	0
Fraction Csp3 :	0.86
Num. rotatable bonds :	6
Num. H-bond acceptors :	2.0
Num. H-bond donors :	0.0
Molar Refractivity :	42.23
TPSA :	26.3 ?2

Pharmacokinetics

GI absorption :	High
BBB permeant :	Yes
P-gp substrate :	No
CYP1A2 inhibitor :	No
CYP2C19 inhibitor :	No
CYP2C9 inhibitor :	No
CYP2D6 inhibitor :	No
CYP3A4 inhibitor :	No
Log Kp (skin permeation) :	-4.83 cm/s

Lipophilicity

Log Po/w (iLOGP) :	2.62
Log Po/w (XLOGP3) :	3.48
Log Po/w (WLOGP) :	2.94
Log Po/w (MLOGP) :	1.96
Log Po/w (SILICOS-IT) :	2.1
Consensus Log Po/w :	2.62

Druglikeness

Lipinski :	0.0
Ghose :	None
Veber :	0.0
Egan :	0.0
Muegge :	1.0
Bioavailability Score :	0.55

Water Solubility

Log S (ESOL) :	-2.66
Solubility :	0.363 mg/ml ; 0.0022 mol/l
Class :	Soluble
Log S (Ali) :	-3.71
Solubility :	0.0318 mg/ml ; 0.000193 mol/l
Class :	Soluble
Log S (SILICOS-IT) :	-2.59
Solubility :	0.426 mg/ml ; 0.00259 mol/l
Class :	Soluble

Medicinal Chemistry

PAINS :	0.0 alert
Brenk :	1.0 alert
Leadlikeness :	1.0
Synthetic accessibility :	1.81

Safety of [ 6092-54-2 ]

Signal Word:	Danger	Class:	6.1,8
Precautionary Statements:	P261-P270-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338	UN#:	3277
Hazard Statements:	H301+H311+H331-H314	Packing Group:	Ⅱ
GHS Pictogram:

Application In Synthesis of [ 6092-54-2 ]

* 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 [ 6092-54-2 ]
Downstream synthetic route of [ 6092-54-2 ]

[ 6092-54-2 ] Synthesis Path-Upstream 1~3

1
[ 75-75-2 ]
[ 6092-54-2 ]
[ 872728-81-9 ]

Reference： [1] Patent: WO2010/45900, 2010, A1, . Location in patent: Page/Page column 10

2
[ 75-75-2 ]
[ 6092-54-2 ]
[ 872728-81-9 ]

Yield	Reaction Conditions	Operation in experiment
35.1 g	Stage #1: With potassium carbonate In water; acetone at 5℃; for 1 h; Stage #2: at 0 - 20℃; for 1 h;	By embodiments 2 - 4 prepared in the target product is 40g adding 3000 ml glass reaction in the bottle, sequentially adding potassium carbonate 33.0g, water 220 ml, acetone 350 ml, stirring the temperature to 5 °C, continuing to stir 10 minutes, slowly instillment chlorine formic acid oneself ester 16.0g, after finishing dropping to continue to 5 °C stirring 1 hours, to the reaction solution is added in dichloromethane 1600 ml, up to 28 °C extracting the organic layer, the saturated salt water for 1600 ml washing, the organic layer is dried with anhydrous sodium sulfate, vacuum concentrated solvent to obtain yellowish liquid. Dichloromethane is used for 80 ml dissolved concentrated residual liquid, adding 1000 ml in the reaction flask, lowering the temperature to 0 °C, in 0 °C slow the instillment uses acetone 640 ml of dissolved methanesulfonic acid 7.7g mixed solution, after the completion of the dropping the temperature to room temperature stirring 1 hour, filtering, dichloromethane 320 ml washing, in 40 °C vacuum drying 5 hours, to obtain 35.1g white compound A, HPLC analysis for 99.789percent

Reference： [1] Patent: CN106397403, 2017, A, . Location in patent: Paragraph 0063; 0064; 0065; 0066; 0067

3
[ 75-75-2 ]
[ 6092-54-2 ]
[ 872728-81-9 ]

Reference： [1] Patent: WO2010/45900, 2010, A1, . Location in patent: Page/Page column 11

[ 6092-54-2 ] Synthesis Path-Downstream 1~6

1
[ 6092-54-2 ]
[ 53279-79-1 ]
[ 60075-91-4 ]

Reference： [1]Journal of Medicinal Chemistry,1976,vol. 19,p. 1362 - 1366

2
[ 75-75-2 ]
[ 6092-54-2 ]
3-({2-[(4-carbamimidoyl-phenylamino)methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}pyridin-2-ylamino)propionic acid ethyl ester hydrochloride [ No CAS ]
[ 872728-81-9 ]

Yield	Reaction Conditions	Operation in experiment
		Preparation of dabigatran mesylate. 9 g of compound VII-HCl (0.017 mol) were dissolved in 300 ml of chloroform. 6, ml of triethylamine were added to this solution and then a solution of 3.4 ml (0.02 mol) of hexyl chloroformate in chloroform was added dropwise. After one hour the reaction mixture is shaken with brine, the organic layer is separated, which is dried with sodium sulfate and concentrated. The obtained evaporation residue is crystallized from ethyl acetate. Yield: 9.6 g (90%)This product is dissolved in acetone and an equimolar amount of methanesulfonic acid is added dropwise. The separated evaporation residue is aspirated and dried at the laboratory temperature. Yield: 73%; content according to HPLC: 99.5%.

Reference： [1]Patent: WO2010/45900,2010,A1 .Location in patent: Page/Page column 11

3
[ 75-75-2 ]
[ 6092-54-2 ]
3-({2-[(4-carbamimidoyl-phenylamino)methyl]-1-methyl-1H-benzoimidazole-5-carbonyl}pyridin-2-yl-amino)-propionic acid ethyl ester dihydrochloride [ No CAS ]
[ 872728-81-9 ]

Yield	Reaction Conditions	Operation in experiment
		Preparation of dabigatran mesylate. To 9.1 g of compound VII-2HC1 (0.016 mol) 270 ml of chloroform and 9 ml (0.064 mol) of triethylamine are added. Then, a solution of 3.1 ml (0.018 mol) of hexyl chloroformate in chloroform is added dropwise at the laboratory temperature. After one hour the reaction mixture is shaken with brine and the organic layer is separated, which is dried with sodium sulfate and concentrated. The obtained evaporation residue is crystallized from ethyl acetate. Yield: 8.6 g (86%)This product is dissolved in acetone and an equimolar amount of methanesulfonic acid is added dropwise. The separated precipitate is aspirated and dried at the laboratory temperature. Yield: 75%; content according to HPLC: 99.5%. 27

Reference： [1]Patent: WO2010/45900,2010,A1 .Location in patent: Page/Page column 10

4
[ 6092-54-2 ]
[ 211915-84-3 ]
[ 872728-81-9 ]

Reference： [1]Patent: WO2013/144903,2013,A1

5
[ 6092-54-2 ]
[ 211915-84-3 ]
[ 211915-06-9 ]

Yield	Reaction Conditions	Operation in experiment
5.3 g		Example 1 : Preparation of beta-Alanine, N-[[2-[[[4-[[[(hexyloxy)carbonyl]amino] iminomethyl] phenyl]amino]methyl]-1 -methyl-1 H-benzimidazol-5-yl]carbonyl]-N-2- pyridinyl-, ethyl ester (dabigatran etexilate) in one pot 1 -Methyl-2-[N-(4-cyanophenyl)-aminomethyl]-benzimidazol-5-yl-carboxylic acid-N-(2-pyridyl)-N-(2-ethoxycarbonylethyl)-amide (10 g) and ethanol (100 mL) were charged into a round bottom flask and cooled to about 5C, dry HCI gas was passed for about 8-10 hours at around 5-10C. The clear solution obtained was maintained for 14-16 hours at 25-30QC for the completion of the reaction and the solution was distilled under reduced pressure at below 40 C. To the crude compound obtained, ethanol (250 mL) and ammonium carbonate (20 g) were charged and the mixture was maintained for 14-16 hours at 25-30QC. To the above obtained reaction mass, water (100 mL) and tetrahydrofuran (200 mL) were charged and the resulting mixture was concentrated under reduced pressure at below 48QC. To the crude obtained, tetrahydrofuran (400 mL), potassium carbonate (18.7 g) were charged followed by slow addition of n-hexyl chloroformate (1 1 .75 g) at 25-30QC and maintained the reaction mass at 25-30QC for around 3 hours. After completion of the reaction, the organic layer was separated and distilled off under reduced pressure. The crude obtained was dissolved in dichloromethane (400 mL) and washed twice with water (2x100 mL) followed by washing twice with 10% sodium chloride solution (2x100 mL) and the layers were separated. The organic layer was concentrated under reduced pressure at below 40QC. To the crude obtained, ethyl acetate (80 mL) was charged and the solid was collected by filtration and washed with ethyl acetate (10 mL). The compound was dried in an oven at 50C for 5 hours to afford the title compound. Yield: 5.3 g; Purity by HPLC: 97.90%.

Reference： [1]Patent: WO2013/144903,2013,A1 .Location in patent: Page/Page column 20

6
[ 75-75-2 ]
[ 6092-54-2 ]
C₂₅H₂₅N₇O₃*C₇H₈O₃S [ No CAS ]
[ 872728-81-9 ]

Yield	Reaction Conditions	Operation in experiment
35.1 g		By embodiments 2 - 4 prepared in the target product is 40g adding 3000 ml glass reaction in the bottle, sequentially adding potassium carbonate 33.0g, water 220 ml, acetone 350 ml, stirring the temperature to 5 C, continuing to stir 10 minutes, slowly instillment chlorine formic acid oneself ester 16.0g, after finishing dropping to continue to 5 C stirring 1 hours, to the reaction solution is added in dichloromethane 1600 ml, up to 28 C extracting the organic layer, the saturated salt water for 1600 ml washing, the organic layer is dried with anhydrous sodium sulfate, vacuum concentrated solvent to obtain yellowish liquid. Dichloromethane is used for 80 ml dissolved concentrated residual liquid, adding 1000 ml in the reaction flask, lowering the temperature to 0 C, in 0 C slow the instillment uses acetone 640 ml of dissolved methanesulfonic acid 7.7g mixed solution, after the completion of the dropping the temperature to room temperature stirring 1 hour, filtering, dichloromethane 320 ml washing, in 40 C vacuum drying 5 hours, to obtain 35.1g white compound A, HPLC analysis for 99.789%

Reference： [1]Patent: CN106397403,2017,A .Location in patent: Paragraph 0063; 0064; 0065; 0066; 0067

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Technical Information

? Acyl Group Substitution ? Alkyl Halide Occurrence ? Bouveault-Blanc Reduction ? Catalytic Hydrogenation ? Complex Metal Hydride Reductions ? Ester Cleavage ? General Reactivity ? Grignard Reaction ? Heat of Combustion ? Hiyama Cross-Coupling Reaction ? Hydride Reductions ? Kinetics of Alkyl Halides ? Kumada Cross-Coupling Reaction ? Preparation of Aldehydes and Ketones ? Reactions of Alkyl Halides with Reducing Metals ? Reactions of Amines ? Reactions with Organometallic Reagents ? Rosenmund Reduction ? Specialized Acylation Reagents-Carbodiimides and Related Reagents ? Specialized Acylation Reagents-Ketenes ? Stille Coupling ? Substitution and Elimination Reactions of Alkyl Halides ? Suzuki Coupling

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[ 6092-54-2 ]

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Ghs Precautionary Statements

Precautionary Statements-General
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.
P211	Do not spray on an open flame or other ignition source.
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
P240	Ground/bond container and receiving equipment.
P241	Use explosion-proof electrical/ventilating/lighting/equipment.
P242	Use only non-sparking tools.
P243	Take precautionary measures against static discharge.
P244	Keep reduction valves free from grease and oil.
P250	Do not subject to grinding/shock/friction.
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.
P265	Wash skin thouroughly after handling.
P270	Do not eat, drink or smoke when using this product.
P271	Use only outdoors or in a well-ventilated area.
P272	Contaminated work clothing should not be allowed out of the workplace.
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.
P283	Wear fire/flame resistant/retardant clothing.
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:
P306	IF ON CLOTHING:
P307	IF exposed:
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. 6092-54-2 ] {[proInfo.proName]}

Quality Control of [ 6092-54-2 ]

Related Doc. of [ 6092-54-2 ]

Product Details of [ 6092-54-2 ]

Calculated chemistry of [ 6092-54-2 ] Expand+

Physicochemical Properties

Pharmacokinetics

Lipophilicity

Druglikeness

Water Solubility

Medicinal Chemistry

Safety of [ 6092-54-2 ]

Application In Synthesis of [ 6092-54-2 ]

[ 6092-54-2 ] Synthesis Path-Upstream 1~3

[ 6092-54-2 ] Synthesis Path-Downstream 1~6

Technical Information

Related Functional Groups of [ 6092-54-2 ]

Aliphatic Chain Hydrocarbons

Chlorides

Acyl Chlorides

Esters

Precautionary Statements-General

Prevention

Response

Storage

Disposal

Physical hazards

Health hazards

Environmental hazards

Inquiry

Related Functional Groups of
[ 6092-54-2 ]