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2(1H)-Pyridinone, 1-methyl-3,4,5,6-tetraphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62557-82-8

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62557-82-8 Usage

Type of compound

Heterocyclic compound

Structure

Contains a pyridinone ring

Substitution

Methyl and four phenyl groups

Usage

Organic synthesis, pharmaceutical research (building block for various organic molecules)

Potential use

Development of new drugs and materials

Biological activities

Investigated for potential therapeutic applications

Check Digit Verification of cas no

The CAS Registry Mumber 62557-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,5 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62557-82:
(7*6)+(6*2)+(5*5)+(4*5)+(3*7)+(2*8)+(1*2)=138
138 % 10 = 8
So 62557-82-8 is a valid CAS Registry Number.

62557-82-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-3,4,5,6-tetraphenylpyridin-2-one

1.2 Other means of identification

Product number -
Other names 1-methyl-3,4,5,6-tetraphenyl-1H-pyridin-2-one

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:62557-82-8 SDS

62557-82-8Downstream Products

62557-82-8Relevant academic research and scientific papers

An Efficient and Novel Approach to the Synthesis of 3,4,5,6-Tetraphenyl-2(1H)-pyridinone

Eagan, Robert L.,Ogliaruso, Michael A.

, p. 1544 - 1547 (2007/10/02)

The reaction of tetracyclone (1a) with sodium azide under acidic conditions was found to give 3,4,5,6-tetraphenyl-2(1H)-pyridinone (2a) in 90percent isolated yield.The reaction does not proceed by a Schmitt mechanism.By adjusting the reaction conditions,

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