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160590-01-2

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160590-01-2 Usage

Molecular weight

235.28 g/mol

Type of compound

Heterocyclic compound

Structure

Contains a pyrrolopyridine ring system

Substituents

A methoxy group at position 7 and a phenyl group at position 3

Usage

Widely used in the pharmaceutical industry as a building block for the synthesis of various bioactive compounds and drug candidates

Biological activities

Exhibits potential anticancer, antimicrobial, and antifungal properties

Potential use

Has been studied for its potential use in the development of new therapeutic agents for various diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 160590-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,5,9 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 160590-01:
(8*1)+(7*6)+(6*0)+(5*5)+(4*9)+(3*0)+(2*0)+(1*1)=112
112 % 10 = 2
So 160590-01-2 is a valid CAS Registry Number.

160590-01-2SDS

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 7-methoxy-3-phenyl-1H-pyrrolo[2,3-c]pyridine

1.2 Other means of identification

Product number -
Other names -

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:160590-01-2 SDS

160590-01-2Downstream Products

160590-01-2Relevant articles and documents

Two-step route to indoles and analogues from haloarenes: A variation on the Fischer indole synthesis

Inman, Martyn,Carbone, Anna,Moody, Christopher J.

, p. 1217 - 1232 (2012/03/26)

In a new variation on the Fischer indole synthesis, readily available haloarenes are converted into a wide range of indoles in just two steps by halogen-magnesium exchange and quenching with di-tert-butyl azodicarboxylate, followed by reaction with aldehy

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