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1H-Indole-2-carbonitrile, 5-chloro-3-(3-nitrophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62039-79-6

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62039-79-6 Usage

Heterocyclic compound

Contains an indole ring The compound is a heterocyclic compound, meaning it has a ring structure containing both carbon and nitrogen atoms, specifically an indole ring.

Cyano group attachment

-C≡N A cyano group (C≡N) is attached to the indole ring, which is a linear triple-bonded nitrogen and carbon group.

Chloro group presence

5-chloro The compound has a chloro group (-Cl) attached to the indole ring at the 5th position, which influences its chemical properties.

Nitrophenyl group presence

3-(3-nitrophenyl) A 3-nitrophenyl group (a phenyl ring with a nitro group -NO2) is attached to the indole ring at the 3rd position.

Potential applications

Pharmaceutical and agrochemical industries The compound may be used as a building block for the synthesis of various bioactive molecules and agrochemicals.

Biological activities

Possible medicinal uses The compound may exhibit biological activities and could be under investigation for its potential medicinal uses.

Check Digit Verification of cas no

The CAS Registry Mumber 62039-79-6 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, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62039-79:
(7*6)+(6*2)+(5*0)+(4*3)+(3*9)+(2*7)+(1*9)=116
116 % 10 = 6
So 62039-79-6 is a valid CAS Registry Number.

62039-79-6SDS

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 5-chloro-3-(3-nitrophenyl)-1H-indole-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 1H-Indole-2-carbonitrile,5-chloro-3-(3-nitrophenyl)

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:62039-79-6 SDS

62039-79-6Upstream product

62039-79-6Downstream Products

62039-79-6Relevant academic research and scientific papers

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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