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142409-79-8

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142409-79-8 Usage

General Description

2,4(1H,3H)-Pyrimidinedione, 1,3-dimethyl-6-[(phenylthio)methyl]- is a chemical compound with the molecular formula C11H12N2O2S. It is a pyrimidinedione derivative with a 1,3-dimethyl-6-[(phenylthio)methyl]- substituent. 2,4(1H,3H)-Pyrimidinedione, 1,3-dimethyl-6-[(phenylthio)methyl]- is potentially useful in various chemical and pharmaceutical applications due to its unique structure and properties. It may have potential uses in drug development or as a building block for the synthesis of other organic compounds. However, the specific uses and properties of this chemical may vary depending on the context and intended application.

Check Digit Verification of cas no

The CAS Registry Mumber 142409-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,4,0 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 142409-79:
(8*1)+(7*4)+(6*2)+(5*4)+(4*0)+(3*9)+(2*7)+(1*9)=118
118 % 10 = 8
So 142409-79-8 is a valid CAS Registry Number.

142409-79-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dimethyl-6-(phenylsulfanylmethyl)pyrimidine-2,4-dione

1.2 Other means of identification

Product number -
Other names -

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

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More Details:142409-79-8 SDS

142409-79-8Downstream Products

142409-79-8Relevant articles and documents

Research on antiviral agents. 5.1 lithiation of 6-methyluracil as a new and efficient entry to C(6)-substituted uracils

Botta, Maurizio,Saladino, Raffaele,Delle Monache, Giuliano,Gentile, Gabriella,Nicoletti, Rosario

, p. 1687 - 1697 (2007/10/03)

Synthesis of numerous C(6)-substituted uracits can be effected by lithiation of N(1), N(3)-substituted 6-methyluracils (1) and (4) with LiHMDS, followed by the reaction of the resulting lithio derivatives with carbon, sulfur, and selenium electrophiles. The unexpected migration of the N(1)-benzoyl group in the melalation-alkylation and the high stereoselectivity obtained in the reaction with substituted cyclohexanones are also reported.

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