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[ CAS No. 46006-36-4 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 46006-36-4
Chemical Structure| 46006-36-4
Structure of 46006-36-4 * Storage: {[proInfo.prStorage]}

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Quality Control of [ 46006-36-4 ]

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Product Details of [ 46006-36-4 ]

CAS No. :46006-36-4 MDL No. :MFCD11656261
Formula : C8H6N2O2 Boiling Point : No data available
Linear Structure Formula :- InChI Key :VVQNAFBGAWCMLU-UHFFFAOYSA-N
M.W : 162.15 Pubchem ID :2771758
Synonyms :

Calculated chemistry of [ 46006-36-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.0
Num. rotatable bonds : 1
Num. H-bond acceptors : 3.0
Num. H-bond donors : 2.0
Molar Refractivity : 43.05
TPSA : 65.98 ?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) : -6.57 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.82
Log Po/w (XLOGP3) : 1.01
Log Po/w (WLOGP) : 1.26
Log Po/w (MLOGP) : 0.58
Log Po/w (SILICOS-IT) : 1.38
Consensus Log Po/w : 1.01

Druglikeness

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

Water Solubility

Log S (ESOL) : -1.97
Solubility : 1.74 mg/ml ; 0.0107 mol/l
Class : Very soluble
Log S (Ali) : -1.98
Solubility : 1.68 mg/ml ; 0.0104 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -2.27
Solubility : 0.863 mg/ml ; 0.00532 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.16

Safety of [ 46006-36-4 ]

Signal Word:Warning Class:
Precautionary Statements:P305+P351+P338 UN#:
Hazard Statements:H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 46006-36-4 ]

* 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 [ 46006-36-4 ]

[ 46006-36-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 64-17-5 ]
  • [ 46006-36-4 ]
  • [ 167487-83-4 ]
YieldReaction ConditionsOperation in experiment
61% Step 1: ethyl 1H-benzimidazole-4-carboxylate 2.50 g (15.4 mmol) 1H-benzimidazole-4-carboxylic acid in 100 mL ethanol are combined with 50 mL saturated ethanolic hydrochloric acid solution and refluxed for 15 hours. The reaction mixture is poured into saturated, aqueous potassium carbonate solution and extracted with ethyl acetate. The combined organic phases are dried on sodium sulphate and evaporated down to 50 mL using the rotary evaporator and filtered. 1.80 g (9.46 mmol, 61%) ethyl 1H-benzimidazole-4-carboxylate are obtained as a colourless solid. Rf=0.92 [silica gel, dichloromethane/methanol (80/20)] MS [ESI (M+H)+]]=191
  • 2
  • [ 51984-63-5 ]
  • [ 46006-36-4 ]
  • 5-chloro-6-methylpyridin-3-yl 1H-benzo[d]imidazole-4-carboxylate [ No CAS ]
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