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143818-35-3

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143818-35-3 Usage

Heterocyclic compound

Contains a pyridinone ring

Substituents

5th carbon atom has an ethyl group, 1st carbon atom has an isopropyl group (1-methylethyl group)

Pharmaceutical intermediate

Used in the synthesis of various drugs

Potential anticonvulsant

May help prevent or reduce the severity of seizures

Potential psychoactive drug

May affect mood, cognition, or behavior

Agricultural applications

Has been studied as a potential pesticide

Industrial applications

May be used in the manufacturing of dyes and pigments

Check Digit Verification of cas no

The CAS Registry Mumber 143818-35-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,8,1 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 143818-35:
(8*1)+(7*4)+(6*3)+(5*8)+(4*1)+(3*8)+(2*3)+(1*5)=133
133 % 10 = 3
So 143818-35-3 is a valid CAS Registry Number.

143818-35-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Ethyl-1-isopropyl-3,4-dihydro-2(1H)-pyridinone

1.2 Other means of identification

Product number -
Other names 5-ethyl-1-isopropyl-3,4-dihydro-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:143818-35-3 SDS

143818-35-3Downstream Products

143818-35-3Relevant articles and documents

Successful thermal rearrangements of acrylenamides to give tetrahydro-2-pyridones under FVT conditions

Lesniak, Stanislaw,Pasternak, Beata

, p. 875 - 880 (2007/10/03)

Enamides of α,β-unsaturated acids are theoretically capable of electrocyclisation to give tetrahydro-2-pyridones. The only successful method reported for this conversion involved photochemical activation. We would like to present new and effective method

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