29943-30-4

Basic information

• Product Name: 2-(Phenylthio)propionyl chloride
• Synonyms: 2-(Phenylthio)propionyl chloride
• CAS NO: 29943-30-4
• Molecular Weight: 200.689
• Mol File: 29943-30-4.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 2-(Phenylthio)propionyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(Phenylthio)propionyl chloride(29943-30-4)
• EPA Substance Registry System: 2-(Phenylthio)propionyl chloride(29943-30-4)

Safety Data

• Hazardous Substances Data: 29943-30-4(Hazardous Substances Data)

Upstream product

• 108-98-5 thiophenol 
• 108-86-1 bromobenzene 
• 17431-94-6 2-phenylsulfanyl-propionic acid 

Downstream Products

• 67175-39-7 1-Diazo-3-phenylthio-2-butanon 
• 129959-68-8 1-tert-Butyl-3-methyl-3-phenylsulfanyl-4-((E)-styryl)-azetidin-2-one 
• 135616-62-5 (3S,4S)-4-Benzoyl-1-(4-methoxy-phenyl)-3-methyl-3-phenylsulfanyl-azetidin-2-one 
• 135616-62-5 (3S,4R)-4-Benzoyl-1-(4-methoxy-phenyl)-3-methyl-3-phenylsulfanyl-azetidin-2-one 
• 135616-48-7 (3S,4S)-1-(4-Methoxy-phenyl)-3-methyl-3-phenylsulfanyl-4-((E)-styryl)-azetidin-2-one 
• 135616-48-7 (3S,4R)-1-(4-Methoxy-phenyl)-3-methyl-3-phenylsulfanyl-4-((E)-styryl)-azetidin-2-one 
• 135616-64-7 (2S,3S)-1-(4-Methoxy-phenyl)-3-methyl-4-oxo-3-phenylsulfanyl-azetidine-2-carboxylic acid methyl ester 
• 135616-64-7 (2R,3S)-1-(4-Methoxy-phenyl)-3-methyl-4-oxo-3-phenylsulfanyl-azetidine-2-carboxylic acid methyl ester 
• 77161-76-3 2,4-bis(phenylthio)-3-pentanone 
• 135616-66-9 (3S,4S)-1-(4-Methoxy-phenyl)-3-methyl-4-phenylethynyl-3-phenylsulfanyl-azetidin-2-one 
• 135616-66-9 (3S,4R)-1-(4-Methoxy-phenyl)-3-methyl-4-phenylethynyl-3-phenylsulfanyl-azetidin-2-one 
• 127055-15-6 (3S,4R)-4-((E)-1,2-Diphenyl-vinyl)-1-(4-methoxy-phenyl)-3-methyl-3-phenylsulfanyl-azetidin-2-one 
• 135616-57-8 (3S,4S)-1-(4-Methoxy-phenyl)-3-methyl-4,5-diphenyl-3,4-dihydro-1H-pyridin-2-one 
• 135616-51-2 (S)-1-(4-Methoxy-phenyl)-3-methyl-4,5-diphenyl-3-phenylsulfanyl-3,4-dihydro-1H-pyridin-2-one 

Relevant articles and documents

Complete assignment of 1H and 13C NMR spectra of some α-arylthio and α-arylsulfonyl substituted N-methoxy-N-methyl propionamides

The complete assignments of the 1H and 13C NMR spectra of the some α-arylthio and α-arylsulfonyl substituted N-methoxy-N-methyl propionamides, bearing methoxy, methyl, chloro, and nitro as substituents at the phenyl ring are reported

Oligomeric aminodiol-containing compounds, libraries thereof, and process of preparing the same

Oligomeric compounds comprising a plurality of aminodiol monomer subunits joined by linking groups are provided, as well as libraries of such compounds and processes for preparing the oligomeric compounds and libraries.

Amine compounds and combinatorial libraries comprising same

The present invention provides monocyclic, bicyclic and oligomeric amine compounds with at least two sites of diversity. These compounds are formed from monocyclic scaffolds which can be cyclized to form bicyclic amine scaffolds. These can then be reacted with building blocks to form the amine compounds of the invention. This invention further provides libraries or monocyclic, bicyclic and oligomeric amine compounds. Also provided are methods for preparing monocyclic, bicyclic and oligomeric amine compounds and libraries thereof. The present invention also provides pharmaceutical compositions of the monocyclic, bicyclic and oligomeric amine compounds.