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3H-Imidazo[4,5-b]pyridine, 3-[(4-bromophenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

161529-30-2

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161529-30-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161529-30-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,5,2 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 161529-30:
(8*1)+(7*6)+(6*1)+(5*5)+(4*2)+(3*9)+(2*3)+(1*0)=122
122 % 10 = 2
So 161529-30-2 is a valid CAS Registry Number.

161529-30-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(4-bromophenyl)methyl]imidazo[4,5-b]pyridine

1.2 Other means of identification

Product number -
Other names 3-(4-bromobenzyl)-3H-imidazo[4,5-b]pyridine

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:161529-30-2 SDS

161529-30-2Relevant academic research and scientific papers

Design, synthesis, and biological evaluation, of the first selective nonpeptide AT2 receptor agonist

Wan, Yiqian,Wallinder, Charlotta,Plouffe, Bianca,Beaudry, Hélène,Mahalingam,Wu, Xiongyu,Johansson, Berndt,Holm, Mathias,Botoros, Milad,Karlén, Anders,Pettersson, Anders,Nyberg, Fred,F?ndriks, Lars,Gallo-Payet, Nicole,Hallberg, Anders,Alterman, Mathias

, p. 5995 - 6008 (2007/10/03)

The first druglike selective angiotensin II AT2 receptor agonist (21) with a Ki value of 0.4 nM for the AT2 receptor and a Ki > 10 μM for the AT1 receptor is reported. Compound 21, with a bioavailability of 20-3

Facile, regioselective syntheses of N-alkylated 2,3-diaminopyridines and imidazo[4,5-b]pyridines

Khanna,Weier,Lentz,Swenton,Lankin

, p. 960 - 965 (2007/10/02)

Useful strategies are reported for the differentiation and selective synthetic manipulations of amino groups at the 2- and 3-positions of pyridines. It has been found that 2,3-diaminopyridine reacts with aldehydes under reductive amination conditions to g

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