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4-Methyl-2-(methylthio)-5-pyrimidinecarbonitrile is a pyrimidine derivative with the molecular formula C7H7N3S. It is a chemical compound that is frequently utilized in the synthesis of pharmaceuticals and agrochemicals. 4-Methyl-2-(methylthio)-5-pyrimidinecarbonitrile is notable for its potential applications in medicinal chemistry, where it serves as a building block for the creation of various biologically active compounds. The presence of the methylthio group in its structure enhances its reactivity and contributes to its potential pharmaceutical properties. Due to its unique structure and pharmacological potential, 4-Methyl-2-(methylthio)-5-pyrimidinecarbonitrile holds a significant position in the realm of organic chemistry and drug discovery.

89079-62-9

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89079-62-9 Usage

Uses

Used in Pharmaceutical Industry:
4-Methyl-2-(methylthio)-5-pyrimidinecarbonitrile is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of biologically active compounds. Its unique structure allows for the creation of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Methyl-2-(methylthio)-5-pyrimidinecarbonitrile is utilized as a precursor in the production of agrochemicals, where its reactivity and chemical properties are leveraged to develop compounds that can protect crops and enhance agricultural productivity.
Used in Medicinal Chemistry Research:
4-Methyl-2-(methylthio)-5-pyrimidinecarbonitrile is employed as a research compound in medicinal chemistry, where scientists explore its potential to form the basis of new drug candidates. Its structural attributes and the presence of the methylthio group make it a valuable tool in the discovery and design of novel therapeutic agents.
Used in Organic Chemistry:
As an organic compound, 4-Methyl-2-(methylthio)-5-pyrimidinecarbonitrile is used in various organic chemistry applications, including the synthesis of complex organic molecules and the study of reaction mechanisms involving pyrimidine derivatives. Its unique properties make it a versatile component in organic synthesis and a subject of interest for chemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 89079-62-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,7 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 89079-62:
(7*8)+(6*9)+(5*0)+(4*7)+(3*9)+(2*6)+(1*2)=179
179 % 10 = 9
So 89079-62-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3S/c1-5-6(3-8)4-9-7(10-5)11-2/h4H,1-2H3

89079-62-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-2-methylsulfanylpyrimidine-5-carbonitrile

1.2 Other means of identification

Product number -
Other names 5-cyano-4-methyl-2-methylthiopyrimidine

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:89079-62-9 SDS

89079-62-9Downstream Products

89079-62-9Relevant academic research and scientific papers

Introduction of Carbon Substituents into Pyrimidines by Grignard Reagents

Rise, Frode,Ongstad, Leif,Gacek, Michel,Undheim, Kjell

, p. 613 - 616 (2007/10/02)

Alkyl- and arylmagnesium halides selectively form 1:1-adducts with the heterocyclic ring in substituted 5-cyanopyrimidines.Dehydrogenation gives the corresponding alkyl or aryl substituted pyrimidine.

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