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2,4(1H,3H)-Pyrimidinedione, 1,3-dimethyl-6-[(phenylthio)methyl]is a pyrimidinedione derivative with a molecular formula of C11H12N2O2S. It features a 1,3-dimethyl-6-[(phenylthio)methyl]substituent, which contributes to its unique structure and properties. This chemical compound is of interest in the fields of chemistry and pharmaceuticals due to its potential applications in drug development and as a building block for synthesizing other organic compounds.

142409-79-8

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142409-79-8 Usage

Uses

Used in Pharmaceutical Industry:
2,4(1H,3H)-Pyrimidinedione, 1,3-dimethyl-6-[(phenylthio)methyl]is used as a potential drug candidate for various therapeutic applications due to its unique chemical structure. Its specific biological activity and mechanism of action may vary depending on the target disease or condition.
Used in Chemical Synthesis:
2,4(1H,3H)-Pyrimidinedione, 1,3-dimethyl-6-[(phenylthio)methyl]serves as a building block for the synthesis of other organic compounds. Its unique structure allows for further chemical modifications and functionalization, enabling the development of new molecules with tailored properties and potential applications in various industries.

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

Emergency phone number -
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More Details:142409-79-8 SDS

142409-79-8Downstream Products

142409-79-8Relevant academic research and scientific papers

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.

PHASE TRANSFER CATALYSED OXIDATIVE ARYLTHIOLATION OF 1,3,6-TRIMETHYLURACIL AND ITS 5-BROMO DERIVATIVE

Kumar, Subodh,Chimni, Swapandeep S.,Cannoo, Deepika

, p. 425 - 428 (2007/10/02)

Reaction of 1,3,6-trimethyluracil and its 5-bromo derivative with arylthiole under phase transfer catalytic conditions provides C-H substitution products, 5-arylthio-1,3,6-trimethyluracils and 5-arylthio-6-arylthiomethyl-1,3-dimethyluracils.

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