37510-36-4

Basic information

• Product Name: methyl 3-hydroxy-3-(p-methylphenyl)prop-2-enedithioate
• Synonyms: methyl 3-hydroxy-3-(p-methylphenyl)prop-2-enedithioate
• CAS NO: 37510-36-4
• Molecular Weight: 224.348
• Mol File: 37510-36-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 3-hydroxy-3-(p-methylphenyl)prop-2-enedithioate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3-hydroxy-3-(p-methylphenyl)prop-2-enedithioate(37510-36-4)
• EPA Substance Registry System: methyl 3-hydroxy-3-(p-methylphenyl)prop-2-enedithioate(37510-36-4)

Safety Data

• Hazardous Substances Data: 37510-36-4(Hazardous Substances Data)

Upstream product

• 2314-48-9 (S,S)-dimethyl trithiocarbonate 
• 122-00-9 para-methylacetophenone 
• 75-15-0 carbon disulfide 
• 74-88-4 methyl iodide 

Downstream Products

• 1142124-89-7 3-(4-methylbenzoyl)-2H-chromene-2-thione 
• 82587-72-2 3-(4-methylbenzoyl)-2H-chromen-2-one 
• 1228956-78-2 3-(4-methylbenzoyl)-8-methoxy-2H-chromene-2-thione 
• 1263317-18-5 3-(4-methylbenzoyl)-6-nitro-2H-chromene-2-thione 
• 1263317-19-6 C₁₇H₁₁NO₅ 
• 1263317-24-3 (3-thioxo-3H-benzo[f]chromen-2-yl)(p-tolyl)methanone 
• 6921-83-1 5-(p-methylphenyl)-3H-1,2-dithiacyclopentene-3-thione 

Relevant articles and documents

Et3N mediated synthesis of polysubstituted thiophenes from α-oxo ketene dithioacetals

In this Letter, an efficient synthetic route to prepare polysubstituted thiophene derivatives was achieved via the Et3N-mediated (Claisen) rearrangement reaction from α-oxo S-methyl-S-propargyl ketenes, which were obtained through alkylation of

An expedient route to highly functionalized 2H-chromene-2-thiones via ring annulation of β-oxodithioesters catalyzed by InCl3 under solvent-free conditions

A convenient and one-pot synthesis of 3-aroyl/heteroaroyl-2H-chromene-2- thiones and benzo[f]2H-chromene-2-thiones has been developed by the condensation of β-oxodithioesters and salicylaldehydes/α-hydroxynaphthaldehydes in the presence of indium trichlor