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118600-53-6

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118600-53-6 Usage

Compound type

Heterocyclic compound

Core structure

Pyrrolopyridine

Substituent

Nitro group attached to the 5th carbon atom

Usage

Building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds

Potential applications

Development of novel drug molecules

Studied for

Anti-cancer and anti-inflammatory properties

Biological activities

May have various activities

Research area

Medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 118600-53-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,6,0 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 118600-53:
(8*1)+(7*1)+(6*8)+(5*6)+(4*0)+(3*0)+(2*5)+(1*3)=106
106 % 10 = 6
So 118600-53-6 is a valid CAS Registry Number.

118600-53-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-nitro-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine

1.2 Other means of identification

Product number -
Other names 5-nitro-7-azaindoline

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:118600-53-6 SDS

118600-53-6Relevant articles and documents

A practical, efficient synthesis of 5-amino-7-azaindole

Pearson, Stuart E.,Nandan, Santosh

, p. 2503 - 2506 (2007/10/03)

A much improved, workable synthesis of 5-amino-7-azaindole is described in 66% overall yield starting from 2-amino-5-nitropyridine. The key stage involves a microwave promoted heteroannulation reaction of a pyridine alkyne. Georg Thieme Verlag Stuttgart.

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