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Ethanone, 1-(1,4-dihydro-6-methyl-2-phenyl-4-thioxo-5-pyrimidinyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81397-23-1

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81397-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81397-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,9 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 81397-23:
(7*8)+(6*1)+(5*3)+(4*9)+(3*7)+(2*2)+(1*3)=141
141 % 10 = 1
So 81397-23-1 is a valid CAS Registry Number.

81397-23-1SDS

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 1-(6-methyl-2-phenyl-4-sulfanylidene-1H-pyrimidin-5-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-(4-methyl-2-phenyl-6-thioxo-1,6-dihydro-5-pyrimidinyl)-1-ethanone

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:81397-23-1 SDS

81397-23-1Relevant academic research and scientific papers

Synthesis and structural studies of 4-thioxopyrimidines with antimicrobial activities

Cunha, Silvio,Bastos, Rodrigo M.,Silva, Priscila De O.,Costa, Giselle A. Nobre,Vencato, Ivo,Lariucci, Carlito,Napolitano, Hamilton B.,De Oliveira, Cecilia M. A.,Kato, Lucilia,Da Silva, Cleuza C.,Menezes, Diego,Vannier-Santos, Marcos A.

, p. 111 - 119 (2007/10/03)

This work describes a two-step, one-pot synthetic method for the formal aza-[3 + 3] cycloaddition between N-alkyl substituted enaminones and benzoyl isothiocyanate, which afforded 4-thioxopyrimidines in reasonable yields. Reaction of acyclic enaminone wit

STUDY OF CYCLIZATION OF 2-ACETYL-3-METHYLAMINO-N-BENZOYL-2-BUTENETHIOAMIDE

Machacek, Vladimir,El-Bahaie, Said,Sterba, Vojeslav

, p. 256 - 261 (2007/10/02)

Kinetics has been studied of cyclization of 2-acetyl-3-methylamino-N-benzoyl-2-butenethioamide (Ia) and 2-acetyl-3-amino-N-benzoyl-2-butenethioamide (Ib) giving 5-acetyl-2-phenyl-1,6-dimethyl-4-(1H)pyrimidinethione (IIa) and 5-acetyl-2-phenyl-6-methyl-4-(

REACTIONS OF CARBONYL ISOTHIOCYANATES WITH ENAMINES OF THE TYPE CH3-C(NH2)=CH-X

Uher, Michal,Ilavsky, Dusan,Foltin, Jozef,Skvareninova, Katarina

, p. 3128 - 3133 (2007/10/02)

Reactions of carbonyl isothiocyanates with enamines of the type CH3-C(NH2)=CH-X (X = CN, COOC2H5, or COCH3) were investigated.The formation of products of AdN, SN, and cyclization reactions is discussed on the basis of their IR, UV a

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