35071-17-1

Usage

Uses

Used in Pharmaceutical Synthesis:
2-Mercapto-4-methylpyrimidine is used as a key building block in the pharmaceutical industry for the synthesis of various drugs. Its presence in the molecular structure of these drugs can contribute to their therapeutic properties and efficacy.
Used in Agrochemical Production:
In the agrochemical sector, 2-Mercapto-4-methylpyrimidine is utilized as a component in the creation of pesticides and other agricultural chemicals, enhancing their effectiveness in protecting crops and managing pests.
Used as a Reagent in Organic Chemical Reactions:
2-Mercapto-4-methylpyrimidine serves as a reagent in organic chemical reactions, particularly for the formation of carbon-sulfur bonds and the synthesis of other thiol-containing compounds. Its reactivity and functional groups make it a valuable tool in organic synthesis.
Used in the Development of Materials and Catalysts:
2-MERCAPTO-4-METHYLPYRIMIDINE has potential applications in the development of new materials and catalysts, where its unique structural features can be leveraged to improve performance or create novel properties in industrial products.

Upstream product

• 5744-65-0 1,1,3,3-tetramethoxy-butane 
• 17356-08-0 thiourea 
• 5436-21-5 acetylacetaldehyde dimethyl acetal 
• 2798-73-4 1-methoxy-buten-3-yne 
• 5424-21-5 2,4-dichloro-6-methylpyrimidine 
• 13036-57-2 2-chloro-4-methylpyrimidine 
• 20082-93-3 3-Oxo-1-phenoxy-buten-⁽¹⁾ 

Downstream Products

• 25710-14-9 N-benzyl-(4-methylpyrimidin-2-yl)amine 
• 1424-14-2 dibenzyl thiourea 
• 216297-14-2 [Ag(triphenylphosphine)2(4-methylpyrimidine-2-thione)2]NO₃ 
• 141463-16-3 [(1S,2R)-1-Cyclohexylmethyl-2-hydroxy-3-(4-methyl-pyrimidin-2-ylsulfanyl)-propyl]-carbamic acid tert-butyl ester 
• 14001-63-9 2-methylthio-4-methylpyrimidine 
• 46118-95-0 (4-methyl-pyrimidin-2-ylsulfanyl)-acetic acid 
• 77166-01-9 4-Methyl-2-(methylsulfonyl)pyrimidine 
• 59215-36-0 1-(4-methyl-pyrimidin-2-yl)piperazine 
• 1338814-07-5 [Au(SC₄H₂N₂Me)(sodium triphenylphosphane monosulfonate)] 
• 218162-50-6 2-thiomethylpyrimidin-4-yl-4-fluorophenylbenzil 
• 217661-99-9 1-(4-fluorophenyl)-2-(2-methylsulphanylpyrimidin-4-yl)-1-ethanone 
• 340042-13-9 3-[2-(Methylsulfonyl)-4-pyrimidinyl]-2-phenylimidazo [1,2-a]pyrimidin-7-amine 
• 340042-11-7 3-[2-(methylthio)-4-pyrimidinyl]-2-phenylimidazo[1,2-a]pyrimidin-7-amine 

Relevant academic research and scientific papers

The reduction of specific disulfides with titanium(III) chloride

The reaction between titanium(III) chloride and disulfides was investigated.Aryl and alkyl disulfides did not react while heterocyclic aromatic disulfides with a nitrogen α to the sulfur were reduced to the corresponding thiols.Products were identified and characterized by nuclear magnetic resonance and inrared spectra; and melting point comparisons with authentic compounds.The reductions occurred only in the presence of citrate and were found to require 2 moles of titanium(III) per mole of disulfide.

7-(3-Substituted ureido) cephalosporins

Cephalosporin compounds with 3-substituted ureido or -thioureido group at position 7 and hydrogen or heterocyclicthiomethyl groups at position 3 are prepared. These compounds are antibacterial agents.