63385-22-8

Basic information

• Product Name: Benzenecarbodithioic acid, 4-methyl-, ethyl ester
• CAS NO: 63385-22-8
• Molecular Formula: C10H12S2
• Molecular Weight: 196.337
• Mol File: 63385-22-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenecarbodithioic acid, 4-methyl-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenecarbodithioic acid, 4-methyl-, ethyl ester(63385-22-8)
• EPA Substance Registry System: Benzenecarbodithioic acid, 4-methyl-, ethyl ester(63385-22-8)

Safety Data

• Hazardous Substances Data: 63385-22-8(Hazardous Substances Data)

Upstream product

• 14062-78-3 N,N-dimethyl-4-toluamide 
• 298-06-6 O,O-Diethyl hydrogen phosphorodithioate 
• 811-51-8 sodium thioethylate 
• 54669-43-1 potassium ethanethiolate 
• 107092-31-9 2-(4-nitrophenyl)vinyl 4-methylbezenecarbonditioate 
• 99-94-5 p-Toluic acid 
• 74670-57-8 cesium 4-methylbenzenecarbodithioate 
• 74670-42-1 potassium 4-methylbenezenecarbodithioate 
• 64-67-5 diethyl sulfate 
• 97270-52-5 4-(methyl)thiobenzoyl diphenylthiophosphinoyl sulfide 
• 30383-01-8 lithium thioethoxide 
• 925-90-6 ethylmagnesium bromide 

Downstream Products

• 1588-49-4 4,4'-dimethylstilbene 
• 538-39-6 1,2-di-p-tolylethane 
• 2789-88-0 1,2-bis(4-methylphenyl)acetylene 
• 69286-83-5 (Z)-Ethylthio-p-tolylsulfin 

Relevant articles and documents

New Synthesis and Some Reactions of Vinyl Arenecarbodithioates. Wittig Reaction of (Triphenylphosphonio)methyl Arenecarbodithioate Iodides

Wittig reaction of new phosphonium salts, (triphenylphosphonio)methyl arenecarbodithioate iodides, with variety of aldehydes gave the corresponding vinyl dithiocarboxylate with nucleophiles such as potassium alkoxide or alkanethiolate was investigated and found to give the thioacylated products in high yields.Ab initio molecular orbital calculations of the model compound vinyl dithioformate, are also discussed.

Raney Nickel Desulphuration of Some Dithioacid Derivatives

Raney Nickel desulphuration of some bisthioaroyl disulphides (I), and lead salts (II) and esters (III) of dithioacids with W-2A, W-2B and W-2C catalysts has been investigated.In some cases dimorphic products are obtained.