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627511-05-1

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627511-05-1 Usage

General Description

2-(4-Bromophenyl)-1H-pyrrolo[2,3-c]pyridine is a chemical compound that belongs to the class of pyrrole-containing heterocycles. It is a fused tricyclic compound that consists of a pyrrole ring fused to a pyridine ring. The 4-bromophenyl group is attached to the pyrrole ring at the 2-position. 2-(4-BROMOPHENYL)-1H-PYRROLO[2,3-C]PYRIDINE has potential applications in medicinal chemistry and drug discovery, as pyrrole-containing compounds often exhibit biological activity and are used as building blocks in the synthesis of pharmaceuticals and biologically active molecules. Its unique structural and chemical properties make it a valuable compound for further research and development in various fields, including organic synthesis, medicinal chemistry, and material science.

Check Digit Verification of cas no

The CAS Registry Mumber 627511-05-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,7,5,1 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 627511-05:
(8*6)+(7*2)+(6*7)+(5*5)+(4*1)+(3*1)+(2*0)+(1*5)=141
141 % 10 = 1
So 627511-05-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H9BrN2/c14-11-3-1-9(2-4-11)12-7-10-5-6-15-8-13(10)16-12/h1-8,16H

627511-05-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-BROMOPHENYL)-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

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More Details:627511-05-1 SDS

627511-05-1Downstream Products

627511-05-1Relevant articles and documents

A novel one-step synthesis of 2-substituted 6-azaindoles from 3-amino-4-picoline and carboxylic esters

Song, Jinhua J.,Tan, Zhulin,Gallou, Fabrice,Xu, Jinghua,Yee, Nathan K.,Senanayake, Chris H.

, p. 6512 - 6514 (2007/10/03)

Dilithiation of 3-amino-4-picoline (1) was achieved with sec-BuLi at room temperature. Condensation of the resulting dianion (2) with carboxylic esters afforded a wide range of 2-substituted 6-azaindoles in good yields.

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