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[ CAS No. 16732-69-7 ] {[proInfo.proName]}

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Chemical Structure| 16732-69-7
Chemical Structure| 16732-69-7
Structure of 16732-69-7 * Storage: {[proInfo.prStorage]}

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Product Details of [ 16732-69-7 ]

CAS No. :16732-69-7 MDL No. :MFCD04972046
Formula : C11H10BrNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :FKIRSCKRJJUCNI-UHFFFAOYSA-N
M.W : 268.11 Pubchem ID :7017885
Synonyms :

Calculated chemistry of [ 16732-69-7 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 15
Num. arom. heavy atoms : 9
Fraction Csp3 : 0.18
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 62.09
TPSA : 42.09 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : Yes
CYP2C9 inhibitor : Yes
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -5.6 cm/s

Lipophilicity

Log Po/w (iLOGP) : 2.69
Log Po/w (XLOGP3) : 3.29
Log Po/w (WLOGP) : 3.11
Log Po/w (MLOGP) : 2.36
Log Po/w (SILICOS-IT) : 3.37
Consensus Log Po/w : 2.96

Druglikeness

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

Water Solubility

Log S (ESOL) : -3.82
Solubility : 0.0405 mg/ml ; 0.000151 mol/l
Class : Soluble
Log S (Ali) : -3.85
Solubility : 0.0379 mg/ml ; 0.000142 mol/l
Class : Soluble
Log S (SILICOS-IT) : -4.62
Solubility : 0.00646 mg/ml ; 0.0000241 mol/l
Class : Moderately soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 0.0
Synthetic accessibility : 1.94

Safety of [ 16732-69-7 ]

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 [ 16732-69-7 ]

* 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 [ 16732-69-7 ]

[ 16732-69-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 617-35-6 ]
  • [ 16732-66-4 ]
  • [ 16732-69-7 ]
YieldReaction ConditionsOperation in experiment
47% toluene-4-sulfonic acid; In toluene; for 16h;Reflux; Water separator; EXAMPLE XIX Ethyl 7-bromo-1H-indole-2-carboxylate 11.0 g <strong>[16732-66-4]2-bromophenylhydrazine</strong> and 550 mg p-toluenesulphonic acid monohydrate are dissolved in 200 ml of toluene, combined with 6.74 ml ethyl pyruvate and refluxed for 2 hours using the water separator. The mixture is allowed to cool to 40 C. and combined with a solution that is obtained by dissolving 44.75 g p-toluenesulphonic acid monohydrate in 300 ml of toluene and refluxing for two hours using the water separator. Then the mixture is refluxed for 12 hours using the water separator. After cooling to ambient temperature the solvents are eliminated in vacuo, the residue is taken up in ethyl acetate and washed successively with water and saturated aqueous sodium hydrogen carbonate solution. After drying with magnesium sulphate the mixture is combined with activated charcoal, stirred for 15 minutes and filtered through kieselguhr. The process of adding activated charcoal, stirring and filtering is repeated twice more. The solvents are eliminated in vacuo and the residue is taken up in petroleum ether/dichloromethane 7:3. 30 g of silica gel are added, the mixture is stirred for 10 minutes and then suction filtered through kieselguhr. The suction filtered silica gel is washed with petroleum ether/dichloromethane 7:3. The solvents are eliminated in vacuo. Yield: 7.37 g (47% of theory) HPLC (method 1): retention time=3.82 min. Mass spectrum (ESI+): m/z=268 [M+H]+
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