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143745-97-5

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143745-97-5 Usage

Aromatic heterocyclic compound

Contains a pyridine ring with attached ethyl and methyl groups

Use in organic synthesis

Commonly used as a building block in organic synthesis

Applications in pharmaceuticals and agrochemicals

Can be found in some pharmaceuticals and agrochemicals

Potential applications in drug production and materials science

Has potential applications in the production of various drugs and in the field of materials science

Biological activity and interest in medicinal chemistry research

May have some biological activity and could be of interest in medicinal chemistry research.

Check Digit Verification of cas no

The CAS Registry Mumber 143745-97-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,7,4 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 143745-97:
(8*1)+(7*4)+(6*3)+(5*7)+(4*4)+(3*5)+(2*9)+(1*7)=145
145 % 10 = 5
So 143745-97-5 is a valid CAS Registry Number.

143745-97-5SDS

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 5-Ethyl-6-methyl-2(1H)-pyridinone

1.2 Other means of identification

Product number -
Other names Asturidon

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:143745-97-5 SDS

143745-97-5Relevant articles and documents

Studies towards 4-C-alkylation of pyridin-2(1H)-one derivatives.

Dolle, Valerie,Nguyen, Chi Hung,Bisagni, Emile

, p. 12505 - 12524 (2007/10/03)

In order to obtain 4-C-alkylated pyridin-2(1H)-ones, two strategies were studied: nucleophilic substitution of 4-chloro-3-nitropyridinone derivatives which essentially failed and lithiations of 2-methoxy-3-pivaloylaminopyridines which gave the expected products.

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