1215940-03-6

Basic information

• Product Name: 1-(4-phenylphenyl)-2-(ethylthio)ethanone
• Synonyms: 1-(4-phenylphenyl)-2-(ethylthio)ethanone
• CAS NO: 1215940-03-6
• Molecular Weight: 256.368
• Mol File: 1215940-03-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(4-phenylphenyl)-2-(ethylthio)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-phenylphenyl)-2-(ethylthio)ethanone(1215940-03-6)
• EPA Substance Registry System: 1-(4-phenylphenyl)-2-(ethylthio)ethanone(1215940-03-6)

Safety Data

• Hazardous Substances Data: 1215940-03-6(Hazardous Substances Data)

Upstream product

• 850998-07-1 2-acetyl-3,3-bis-ethylsulfanyl-N-o-tolyl-acrylamide 
• 135-73-9 2-Bromo-4'-phenylacetophenone 

Relevant articles and documents

An efficient and odorless synthesis of thioethers using 2-[Bis(alkylthio)methylene]-3-oxo-N-o-tolylbutanamides as thiol equivalents

Using 2-[bis(alkylthio)methylene]-3-oxo-N-o-tolylbutanamides 1 as odorless thiol equivalents, an efficient and odorless synthesis of thioethers has been developed. Promoted by NaOH in EtOH, the cleavage of 1 commences to generate thiolate anions, and the generated thiolate anions then react with halides to give various thioethers in good yield. It is noteworthy that only a very faint odor of thiols can be perceived during both the reaction and the workup. Using 2-[bis(alkylthio)methylene]-3-oxo-N-o-tolylbutanamides as odorless thiol equivalents, an efficient and odorless synthesis of thioethers has been developed. Promoted by NaOH in EtOH, the cleavage of 2-[bis(alkylthio)methylene] -3-oxo-N-o-tolylbutanamides commences to generate thiolate anions, and the generated thiolate anions then react with halides to give various thioethers in good yield. Copyright