60410-77-7

Upstream product

• 2168-80-1 4-methyldithioic acid 
• 64586-19-2 Acetic 4-methylthiobenzoic thioanhydride 
• 39969-71-6 S-phenylcarbamoyl 4-methyldithiobenzoate 
• 80047-73-0 (4-methylbenzoyl)(4-methylbenzenecarbothioyl) sulfide 
• 14338-32-0 2-chloro-1-methyl-pyridinium iodide 
• 42967-76-0 piperidinium 4-methylbenzenecarbodithiolate 
• 74670-42-1 potassium 4-methylbenezenecarbodithioate 
• 129256-82-2 1-methyl-2-<4-methylphenyl(thiocarbonylthio)>pyridinium iodide 
• 53724-36-0 sodium 4-(methyl)dithiobenzoate 
• 78923-70-3 4-Methylbenzoyl 4-methyl-thiobenzoyl disulfide 

Downstream Products

• 83078-38-0 4-Methyl-dithiobenzoic acid; compound with morpholine 
• 61750-20-7 morpholino(p-tolyl)methanethione 
• 83078-41-5 4-Methyl-thiobenzoic acid O-p-tolyl ester 
• 99-75-2 4-methyl-benzoic acid methyl ester 
• 5977-80-0 O-methyl 4-methylbenzenecarbothioate 
• 53724-36-0 sodium 4-(methyl)dithiobenzoate 
• 94-08-6 4-methylbenzoic acid ethyl ester 
• 26028-04-6 O-ethyl 4-methylbenzenecarbothioate 
• 19277-55-5 isopropyll 4-methylbenzoate 
• 83078-40-4 4-methyl-thiobenzoic acid O-isopropyl ester 
• 52322-79-9 O-phenyl 4-methylbenzenecarbothioate 
• 20849-31-4 4-Methyldithiobenzoesaeurephenylester 
• 120449-42-5 Se-phenyl 4-methylbenzenecarboselenothioate 
• 5467-99-2 4-methylbenzoic acid benzyl ester 

Relevant academic research and scientific papers

A Convenient Preparation of Bis(thioacyl) Sulfides

Bis(thioacyl) sulfides are prepared in 60-90percent yield in a one-pot reaction of piperidinium or alkali metal dithiocarboxylates with 2-chloro-1-methylpyridinium iodide at room temperature.

Preparation and Some Reactions of Bis(thioacyl) Sulfides

Reaction of dithioic acids with dicyclohexylcarbodiimide has been found to give the corresponding bis(thioacyl) sulfides 1 in good yield, which are very useful thioacylating reagents under mild reaction conditions.Most of the aromatic thioanhydrides (1, R = aromatic) are fairly stable green crystals at room temperature, but the aliphatic ones (1, R = aliphatic) are unstable purple oils which dimerize at room temperature to give the dithietanes 5.The reactions with nucleophiles are discussed.

The Preparation and Some Reactions of Unsymmetrical Acyl Thioacyl Sulfides

A number of unsymmetrical acyl thioacyl sulfides have been prepared and characterized by the reaction of piperidinium or sodium dithiocarboxylates with acyl chlorides or by desulfurization reaction of acyl thioacyl disulfides with triphenylphosphine.They are deep blue oils or light green crystals and very unstable thermally and for moisture.The n --> ?* transitions of the thiocarbonyl group of 1 appear in higher wave length region than those of the corresponding symmetrical bis(thioacyl) sulfides .Some reactions with nucleophiles are discussed.It was found that the symmetricallization reaction of these unsymmetrical acyl thioacyl sulfides occurs in the presence of base such as lithium ethanethiolate to give the symmetrical bis(thioacyl) disulfides in fair yield.