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62039-80-9

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62039-80-9 Usage

Molecular Weight

313.33 g/mol

Structure

An indole ring with a fluorine atom at the 6th position, a carbonitrile group at the 2nd position, and a 4-methoxyphenyl substituent at the 3rd position.

Fluorine atom

Present at the 6th position of the indole ring.

Carbonitrile group

Present at the 2nd position of the indole ring.

Methoxy group

Present at the 4th position of the phenyl ring.

Biological Activity

Used as a building block in the synthesis of various biologically active molecules.

Medicinal Chemistry

Valued precursor in the development of potential drug candidates.

Pharmaceutical Research

Targeting various biological pathways with its unique structure and functional groups.

Check Digit Verification of cas no

The CAS Registry Mumber 62039-80-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,3 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62039-80:
(7*6)+(6*2)+(5*0)+(4*3)+(3*9)+(2*8)+(1*0)=109
109 % 10 = 9
So 62039-80-9 is a valid CAS Registry Number.

62039-80-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-fluoro-3-(4-methoxyphenyl)-1H-indole-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 1H-Indole-2-carbonitrile,6-fluoro-3-(4-methoxyphenyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:62039-80-9 SDS

62039-80-9Upstream product

62039-80-9Downstream Products

62039-80-9Relevant articles and documents

Preparation of indole derivatives

-

, (2008/06/13)

An improved process for preparing indole derivatives of the formula, STR1 wherein R1 and R2 each are hydrogen, halogen, C1 -C3 alkyl, C1 -C3 alkoxy, nitro, cyano or trifluoromethyl, or when taken together, form methylenedioxy; R3 is hydrogen, halogen, C1 -C3 alkyl, C1 -C3 alkoxy, nitro, cyano or dimethylamino; and R4 is hydrogen or halogen, which comprises cyclizing a compound of the formula, STR2 wherein R1, R2, R3 and R4 are as defined above, with an acidic condensing agent. The indole derivatives of the formula (I) mentioned above are useful as a key intermediate for the preparation of benzodiazepines, which are useful as tranquilizers, muscle relaxants and the like.

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