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2-Propen-1-one, 3-phenyl-1-(2-phenylimidazo[1,2-a]pyridin-3-yl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62472-27-9

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62472-27-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62472-27-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,7 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62472-27:
(7*6)+(6*2)+(5*4)+(4*7)+(3*2)+(2*2)+(1*7)=119
119 % 10 = 9
So 62472-27-9 is a valid CAS Registry Number.

62472-27-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-1-(2-phenylimidazo[1,2-a]pyridin-3-yl)prop-2-en-1-one

1.2 Other means of identification

Product number -
Other names 2-Phenyl-3-cinnamoylimidazo<1,2-a>pyridin

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:62472-27-9 SDS

62472-27-9Downstream Products

62472-27-9Relevant academic research and scientific papers

Copper(II)-catalyzed aerobic oxidative coupling between chalcone and 2-aminopyridine via C-H amination: An expedient synthesis of 3-aroylimidazo[1,2-a]pyridines

Monir, Kamarul,Kumar Bagdi, Avik,Mishra, Subhajit,Majee, Adinath,Hajra, Alakananda

, p. 1105 - 1112 (2014)

A simple and efficient protocol has been developed for the synthesis of 3-aroylimidazopyridines via copper(II) acetate-catalyzed aerobic oxidative amination. A library of 3-aroylimidazopyridines was synthesized from readily accessible chalcones and 2-aminopyridines with high yields and regioselectivity. The reaction proceeds through a tandem Michael addition followed by an intramolecular oxidative amination. The successful application of this methodology for a gram-scale reaction indicates its potential for bulk synthesis.

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