56974-15-3

Basic information

• Product Name: Hexanethioic acid, S-phenyl ester
• CAS NO: 56974-15-3
• Molecular Formula: C12H16OS
• Molecular Weight: 208.324
• Mol File: 56974-15-3.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Hexanethioic acid, S-phenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Hexanethioic acid, S-phenyl ester(56974-15-3)
• EPA Substance Registry System: Hexanethioic acid, S-phenyl ester(56974-15-3)

Safety Data

• Hazardous Substances Data: 56974-15-3(Hazardous Substances Data)

Upstream product

• 123-66-0 Ethyl hexanoate 
• 15821-77-9 Aluminium tris(phenylthiolate) 
• 13464-19-2 phenyl chlorothioformate 
• 693-25-4 n-pentylmagnesium bromide 
• 108-98-5 thiophenol 
• 142-62-1 hexanoic acid 
• 931-59-9 benzenesulfenyl chloride 
• 693-02-7 hex-1-yne 
• 120346-63-6 (E)-3-butyl-2-phenylsulphonyl-2-phenylthiooxirane 
• 120346-59-0 (E)-1-phenylsulphonyl-1-phenylthiohex-1-ene 
• 15296-86-3 1-(phenylsulfanyl)methyl phenyl sulfone 
• 35453-12-4 phenyl phenylthiomethyl sulfoxide 
• 3561-67-9 bis(phenylthio)methane 
• 110-62-3 pentanal 

Downstream Products

• 942-92-7 caprophenone 
• 927-49-1 dipentyl ketone 
• 621-15-8 N-(n-hexanoyl)aniline 

Relevant articles and documents

Beta-lactones as antibacterial agents

The present invention relates to specific beta-lactone compounds and compositions thereof for the treatment of infections, such as, e.g., infections with bacteria or infections with protozoa, in particular infections with Gram-positive and/or Gram-negativ

β-lactones as privileged structures for the active-site labeling of versatile bacterial enzyme classes

(Chemical Equation Presented) A chemical proteomic strategy has been applied directly to bacterial proteomes, and b-lactones have been identified as important natural product derivatives with a high affinity to various enzyme classes (see picture). This a

Cleavage of S-S bond by Sm/cat. CoCl2 or Sm/cat. CoCl2 · 6H2O system. A novel method for the synthesis of thiolesters

The Sm/cat. CoCl2 or Sm/cat. CoCl2 · 6H2O system promoted dlsulfides to react with anhydrides or acyl chlorides to afford thiolesters in good yields under mild and neutral conditions.