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[ CAS No. 46004-37-9 ] {[proInfo.proName]}

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Chemical Structure| 46004-37-9
Chemical Structure| 46004-37-9
Structure of 46004-37-9 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 46004-37-9 ]

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Product Details of [ 46004-37-9 ]

CAS No. :46004-37-9 MDL No. :MFCD03840484
Formula : C8H8ClNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :DSHBGNPOIBSIOQ-UHFFFAOYSA-N
M.W : 185.61 Pubchem ID :11839197
Synonyms :

Calculated chemistry of [ 46004-37-9 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.12
Num. rotatable bonds : 2
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 47.14
TPSA : 52.32 ?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) : -6.25 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.71
Log Po/w (XLOGP3) : 1.66
Log Po/w (WLOGP) : 1.72
Log Po/w (MLOGP) : 1.91
Log Po/w (SILICOS-IT) : 1.61
Consensus Log Po/w : 1.72

Druglikeness

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

Water Solubility

Log S (ESOL) : -2.27
Solubility : 0.986 mg/ml ; 0.00531 mol/l
Class : Soluble
Log S (Ali) : -2.37
Solubility : 0.787 mg/ml ; 0.00424 mol/l
Class : Soluble
Log S (SILICOS-IT) : -2.73
Solubility : 0.344 mg/ml ; 0.00185 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.42

Safety of [ 46004-37-9 ]

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

Application In Synthesis of [ 46004-37-9 ]

* 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.

  • Downstream synthetic route of [ 46004-37-9 ]

[ 46004-37-9 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 46004-37-9 ]
  • [ 117738-77-9 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; sodium carbonate; sodium nitrite; In water; ethyl acetate; EXAMPLE 75 2-Chloro-4-cyanobenzoic Acid, Methyl Ester 2-chloro-4-aminobenzoic acid, methyl ester (13.95 g) was suspended in a mixture of water (65 ml) and concentrated hydrochloric acid (15.7 ml). After stirring at room temperature for 10 minutes, the suspension was cooled to 0 C. A solution of sodium nitrite (5.71 g) in water (37 ml) was gradually added over 20 minutes, maintaining a reaction temperature of 0 C. After stirring at 0 C. for 35 minutes, the reaction mixture was partially neutralized by the addition of solid sodium carbonate (3.16 g) to afford a cold solution of the diazonium salt. To a pre-cooled solution of copper(I) cyanide (8.4 g) and sodium cyanide (9.19 g) in water (112 ml) was gradually added the above solution of diazonium salt over a 45-50 minute period. The diazonium salt solution was maintained at 0 C. during the addition. The resulting mixture was stirred for 18 hours at room temperature. A precipitate was filtered, air-dried, dissolved in ethyl acetate (250 ml), and filtered to remove insoluble matter. The organic phase was dried over anhydrous magnesium sulfate, and the solvent removed in vacuo to afford a crude product as a brown solid (13.2)g). The crude product was purified by column chromatography on silica gel (250 g), eluding with 5-10% ethyl acetate/hexane to yield the title compound (10.9 g) as a solid, m.p. 90-92 C.; MS (EI), m/z: 195 (M)+.
  • 2
  • [ 46004-37-9 ]
  • [ 162100-83-6 ]
  • 3
  • [ 46004-37-9 ]
  • [ 20605-41-8 ]
  • C11H8ClN3O3 [ No CAS ]
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