60718-19-6

Basic information

• Product Name: Propanethioic acid, 2,2-dimethyl-, S-phenyl ester
• Synonyms: 2,2-Dimethylpropionyl-phenyl-thioether;2,2-dimethylthiopropionic acid S-phenyl ester;Propanethioic acid,2,2-dimethyl-,S-phenyl ester;S-phenyl 2,2-dimethylpropanethiolate
• CAS NO: 60718-19-6
• Molecular Formula: C11H14OS
• Molecular Weight: 194.298
• Mol File: 60718-19-6.mol
• Article Data: 19

Chemical Properties

• CAS DataBase Reference: Propanethioic acid, 2,2-dimethyl-, S-phenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Propanethioic acid, 2,2-dimethyl-, S-phenyl ester(60718-19-6)
• EPA Substance Registry System: Propanethioic acid, 2,2-dimethyl-, S-phenyl ester(60718-19-6)

Safety Data

• Hazardous Substances Data: 60718-19-6(Hazardous Substances Data)

Upstream product

• 201230-82-2 carbon monoxide 
• 882-33-7 diphenyldisulfane 
• 4551-15-9 phenylthiotrimethylsilane 
• 37170-49-3 trimethylsilyl 2,2-dimethylpropionate 
• 27644-18-4 pivaloyl bromide 
• 1192-40-1 copper(I) thiophenolate 
• 108-98-5 thiophenol 
• 75-98-9 Trimethylacetic acid 
• 3282-30-2 pivaloyl chloride 
• 1503-86-2 2-naphthyl pivalate 
• 13464-19-2 phenyl chlorothioformate 
• 558-17-8 tert-Butyl iodide 
• 111248-35-2 2-pivaloyloxyacrylonitrile 
• 343220-59-7 2,4,6-trichlorobenzoic pivalic anhydride 

Downstream Products

• 882-33-7 diphenyldisulfane 
• 7570-96-9 2-naphthyl phenyl sulfide 
• 14248-22-7 methyl 2,2-dimethyl-3-phenylpropionate 
• 100-68-5 methyl-phenyl-thioether 

Relevant articles and documents

Manganese(iii)-promoted thiocarbonylation of alkylborates with disulfides: synthesis of aliphatic thioesters

A Mn(iii)-promoted thiocarbonylation procedure toward the synthesis of thioesters has been developed. By employing easily available disulfides and potassium alkyltrifluoroborates as the starting materials, and cheap and non-toxic Mn(OAc)3·2H2O as the promotor, a broad range of thioesters were synthesized in good to excellent yieldsviaradical intermediates.

Synthesis of thiol esters using nano CuO/Ionic liquid as an eco-friendly reductive system under microwave irradiation

We report an efficient, fast, and environmentally friendly method for the synthesis of a wide range of thiol esters using stable diorganoyl disulfides and acyl chlorides, using CuO nanoparticles and [pmim]Br as the reductive system. This method gave good to excellent isolated yields of the desired products after only three minutes of microwave irradiation. Furthermore, by using the same green approach, we were also able to synthesize thiocarbonates bearing interesting functionalities. We report an efficient, fast, and environmentally friendly method for the synthesis of thiol esters starting from diorganoyl disulfides and acyl chlorides, and using CuO nanoparticles and [pmim]Br as the reductive system. This approach gave good to excellent isolated yields of the desired products in only three minutes under microwave irradiation. Copyright

Synthesis of thiol esters by the reaction of ricinoleic acid with thiols under solvent-free conditions

The synthesis of several ricinoleic acid thiol esters starting from cis-(R)-12-hydroxyoctadec-9-enoic acid and thiols in the presence of N,N'-dicyclohexylcarbodiimide (DCC) is described. The method is efficient for aromatic and aliphatic thiols, selective