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250651-52-6

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250651-52-6 Usage

General Description

The chemical 1H-Imidazo[4,5-b]pyridine-2-methanol, -alpha--methyl- (9CI) is a heterocyclic compound with a pyridine ring fused to an imidazole ring. It also contains a methanol group and a methyl group attached to the alpha carbon of the imidazole ring. This chemical is commonly used in the pharmaceutical industry as a building block for the synthesis of various pharmaceutical drugs and compounds. Its unique structure and properties make it valuable for medicinal and research purposes, particularly in the development of novel drugs with potential therapeutic applications. Additionally, it is also used as a reagent in organic synthesis for the preparation of various compounds with diverse functional groups.

Check Digit Verification of cas no

The CAS Registry Mumber 250651-52-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,0,6,5 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 250651-52:
(8*2)+(7*5)+(6*0)+(5*6)+(4*5)+(3*1)+(2*5)+(1*2)=116
116 % 10 = 6
So 250651-52-6 is a valid CAS Registry Number.

250651-52-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1-hydroxyethyl)-1H-imidazo[4,5-b]pyridine

1.2 Other means of identification

Product number -
Other names 1-(3H-imidazo[4,5-b]pyridin-2-yl)-ethanol

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:250651-52-6 SDS

250651-52-6Relevant articles and documents

Lithium bromide catalyzed solvent free method for synthesis of 2-substituted benzimidazoles and imidazopyridines

Dekhane, Deepak V.,Pawar, Shivaji S.,Gupta, Sunil V.,Shingare, Murlidhar S.,Thore, Shivaji N.

experimental part, p. 519 - 523 (2011/01/13)

The first successful lithium bromide mediated solvent free condensation of arylenediamine and esters to obtain 2-substituted benzimidazole and imidazopyridine in good to excellent yields is described.

Synthesis and some reactions of 2-acetylimidazo[4,5-b]pyridine. Antituberculotic activity of the obtained compounds

Bukowski,Janowiec,Zwolska-Kwiek,Andrzejczyk

, p. 651 - 654 (2007/10/03)

2-Acetylimidazo[4,5-b]pyridine was prepared and its reactions with some aromatic amines and sulfur (Willgerodt-Kindler reaction), some aromatic aldehydes, some carboxylic acid hydrazides as well as thiourea were investigated. New imidazo[4,5-b]pyridine derivatives with different substituents in 2-position (N-arylthioamides, imines, α β-unsaturated ketones, hydrazido-hydrazones and aminothiazole) were obtained. Most of the synthesized compounds were tested in vitro for their antituberculotic activity.

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