638-13-1

Basic information

• Product Name: 4-Methyl-6-mercapto-2-pyrimidinol
• Synonyms: 2(1H)-Pyrimidinone, 3,4-dihydro-6-methyl-4-thioxo- (9CI);4-Mercapto-6-MethylpyriMidin-2(1H)-one;6-Methyl-4-thioxo-3,4-dihydropyriMidin-2(1H)-one;3,4-Dihydro-6-methyl-4-thioxo-2(1H)-pyrimidinone;6-methyl-4-sulfanylidene-1,2,3,4-tetrahydropyrimidin-2-one
• CAS NO: 638-13-1
• Molecular Formula: C₅H₆N₂OS
• Molecular Weight: 142.17894
• Product Categories: PYRIMIDINE
• Mol File: 638-13-1.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 387.8°C at 760 mmHg
• Flash Point: 188.4°C
• Appearance: /
• Density: 1.36g/cm³
• Vapor Pressure: 1.43E-06mmHg at 25°C
• Refractive Index: 1.638
• CAS DataBase Reference: 4-Methyl-6-mercapto-2-pyrimidinol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Methyl-6-mercapto-2-pyrimidinol(638-13-1)
• EPA Substance Registry System: 4-Methyl-6-mercapto-2-pyrimidinol(638-13-1)

Safety Data

• Hazardous Substances Data: 638-13-1(Hazardous Substances Data)

Usage

General Description

4-Methyl-6-mercapto-2-pyrimidinol is a chemical compound with the molecular formula C5H6N2OS. It is a pyrimidine derivative, and it contains a methyl group and a thiol group. 4-Methyl-6-mercapto-2-pyrimidinol has been studied for its potential use in pharmaceuticals, and it may have antioxidant and chelating properties. It may also be used in the synthesis of other organic compounds. Additionally, it has been investigated for its potential use in corrosion inhibition and as a potential treatment for various diseases. Overall, 4-Methyl-6-mercapto-2-pyrimidinol is a versatile compound with potential applications in various fields.

InChI:InChI=1/C5H6N2OS/c1-3-2-4(9)7-5(8)6-3/h2H,1H3,(H2,6,7,8,9)

Upstream product

• 626-48-2 6-Methyluracil 
• 6310-04-9 2-(Methylthio)-6-methyl-pyrimidin-thiol-(4) 

Downstream Products

• 78932-30-6 6-Methyl-4-(4-nitro-benzylsulfanyl)-1H-pyrimidin-2-one 
• 127067-01-0 6-Methyl-4-{4-[4-((E)-styryl)-phenoxy]-butylsulfanyl}-1H-pyrimidin-2-one 
• 127067-02-1 6-Methyl-4-{5-[4-((E)-styryl)-phenoxy]-pentylsulfanyl}-1H-pyrimidin-2-one 
• 127067-03-2 6-Methyl-4-{6-[4-((E)-styryl)-phenoxy]-hexylsulfanyl}-1H-pyrimidin-2-one 
• 78932-28-2 4-Benzylsulfanyl-6-methyl-1H-pyrimidin-2-one 
• 42351-98-4 4-hydrazinyl-6-methylpyrimidin-2(1H)-one 
• 16710-13-7 6-methyluridine 
• 99284-28-3 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-4-(methylthio)-6-methyluracil 
• 16710-11-5 6-methyl-4-(methylsulfanyl)pyrimidin-2(1H)-one 

Relevant articles and documents

HETEROARYL DERIVATIVES AS SEPIAPTERIN REDUCTASE INHIBITORS

Inhibitors of sepiapterin reductase of formula (I) or (I'), wherein the substituents are defined as in the claims, and uses of sepiapterin reductase inhibitors in analgesia, treatment of acute and chronic pain, anti-inflammation, and immune cell regulation are disclosed.

4-arylamino-2-(2-acetoxyethyl)amino-6-methylpyrimidines: Synthesis, deacetylation, and biological activity

The reaction of 2-(2-acetoxyethyl)amino-4-chloro-6-methylpyrimidine with aromatic amines leads to a series of 4-arylamino-2-(2-acetoxyethyl)amino-6- methylpyrimidines. Deacetylation of these compounds proceeds in both acidic and basic media. Most of the a

Bis-s-triazolopyrimidine and Some Simple Derivatives

A general synthetic route to the new tricyclic system bis-s-triazolopyrimidine, is reported.Thus the parent heterocycle (11a) is prepared from the key bicyclic intermediate, s-triazolopyrimidin-5-ylamine (7a), through the correspondi