56379-68-1

Basic information

• Product Name: S-phenyl thio-n-valerate
• Synonyms: S-phenyl thio-n-valerate
• CAS NO: 56379-68-1
• Molecular Weight: 194.298
• Mol File: 56379-68-1.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: S-phenyl thio-n-valerate(CAS DataBase Reference)
• NIST Chemistry Reference: S-phenyl thio-n-valerate(56379-68-1)
• EPA Substance Registry System: S-phenyl thio-n-valerate(56379-68-1)

Safety Data

• Hazardous Substances Data: 56379-68-1(Hazardous Substances Data)

Upstream product

• 100693-33-2 1-cyclohexene 
• 638-29-9 n-valeryl chloride 
• 108-98-5 thiophenol 
• 56819-74-0 methyl phenyl sulfide α-carbanion 
• 79597-48-1 1-cyclohexenylmethyl phenyl sulfide 
• 444343-55-9 butyltrifluoro-λ⁴-borane potassium salt 
• 201230-82-2 carbon monoxide 
• 882-33-7 diphenyldisulfane 
• 542-69-8 1-iodo-butane 
• 109-65-9 1-bromo-butane 
• 110-62-3 pentanal 
• 100-68-5 methyl-phenyl-thioether 
• 624-24-8 methyl valerate 
• 109-52-4 valeric acid 

Downstream Products

• 1052108-48-1 C₁₇H₂₄O₂S 
• 78839-95-9 1-(phenylethynyl)-1-pentenyl phenyl sulfide 
• 78839-93-7 (E)-1-butylidene-2-heptenyl phenyl sulfide 
• 78839-94-8 1-ethyl-1-pentenyl phenyl sulfide 
• 78839-96-0 (E/Z)-pent-1-enyl phenyl sulfide 
• 20032-49-9 1-methyl-1-pentenyl phenyl sulfide 
• 591-78-6 n-hexan-2-one 
• 78839-91-5 1-phenylthio-1-pentenyl diphenyl phosphate 
• 6225-06-5 N,N-dimethylpentanamide 

Relevant articles and documents

Tetraethylammonium bromide-catalyzed oxidative thioesterification of aldehydes and alcohols

A metal-free, tetraethylammonium bromide-catalyzed oxidative coupling of aldehydes or alcohols with thiophenols or disulfides has been developed. This protocol affords an efficient and inexpensive approach to the synthesis of a wide range of thioesters in high yields. Copyright

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.

Rapid and convenient thioester synthesis under phase-transfer catalysis conditions

Various thioesters were obtained through an efficient phase-transfer catalysis method, by treating several thiophenols with different acyl chlorides, in a biphasic system composed of 10% aqueous NaOH and dichloromethane in the presence of tetrabutylammonium chloride. The thiolation reaction was complete in only 5 minutes, at 0C. Taylor & Francis Group, LLC.