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Imidazo[1,2-a]pyridine-6-carboxylic acid, 8-amino-2,3-dimethyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

248919-96-2

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248919-96-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 248919-96-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,8,9,1 and 9 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 248919-96:
(8*2)+(7*4)+(6*8)+(5*9)+(4*1)+(3*9)+(2*9)+(1*6)=192
192 % 10 = 2
So 248919-96-2 is a valid CAS Registry Number.

248919-96-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-amino-2,3-dimethyl-imidazo[1,2-a]pyridine-6-carboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names methyl 8-amino-2,3-dimethylimidazo[1,2-a]pyridine-6-carboxylate

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:248919-96-2 SDS

248919-96-2Relevant academic research and scientific papers

Novel indanyl-substituted imidazo[1,2-a]pyridines as potent reversible inhibitors of the gastric H+/K+-ATPase

Zimmermann, Peter Jan,Buhr, Wilm,Brehm, Christof,Palmer, Andreas Marc,Feth, Martin Philipp,Senn-Bilfinger, Joerg,Simon, Wolfgang-Alexander

, p. 5374 - 5378 (2008/09/21)

A series of novel 8-indanylamino- and 8-indanyloxy-substituted imidazo[1,2-a]pyridines with reduced lipophilicity was synthesized from easily accessible starting compounds. The anti-secretory activity of these compounds has been assessed in a competitive

Process for preparing a substituted imidazopyridine compound

-

, (2008/06/13)

The present invention provides a new process for large-scale preparation of substituted imidazopyridine compound of formula (1) wherein R1 is C1-C6 alkoxy or NH2 group, comprising the step of reacting a compound of formula (2) with a 3-halo-2-butanone compound in cyclohexanone.

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