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Imidazo[1,2-a]pyridine, 5-(1-methylethyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78132-61-3

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78132-61-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78132-61-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,1,3 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 78132-61:
(7*7)+(6*8)+(5*1)+(4*3)+(3*2)+(2*6)+(1*1)=133
133 % 10 = 3
So 78132-61-3 is a valid CAS Registry Number.

78132-61-3SDS

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 5-Isopropyl-imidazo[1,2-a]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:78132-61-3 SDS

78132-61-3Downstream Products

78132-61-3Relevant academic research and scientific papers

TRANSMISSION D'UN EFFET STERIQUE PERI A TRAVERS UN NOYAU HETEROAROMATIQUE-I SYNTHESE ET PROPRIETES SPECTRALES DE DIALKYLIMIDAZO a>PYRIDINES PERI DISUBSTITUEES

Maury, G.,Pigiere, C.

, p. 83 - 90 (1981)

The regiospecificity of the condensation of 2-amino-pyridines and α-halo carbonyl compounds has been established and exists even in the occurrence of steric effects.Using this regiospecificity peri disubstituted imidazoa>pyridines have been prepared. (13)C and P NMR studies show profound differences between the spectra of peri disubstituted compounds and other disubstituted imidazoa>pyridines.These differences have been interpreted in terms of peri steric effects; preferential conformations of the peri alkyl substituents are postulated.

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