77331-03-4

Basic information

• Product Name: Propanal, 2,2-bis(phenylthio)-
• CAS NO: 77331-03-4
• Molecular Formula: C15H14OS2
• Molecular Weight: 274.408
• Mol File: 77331-03-4.mol

Chemical Properties

• CAS DataBase Reference: Propanal, 2,2-bis(phenylthio)-(CAS DataBase Reference)
• NIST Chemistry Reference: Propanal, 2,2-bis(phenylthio)-(77331-03-4)
• EPA Substance Registry System: Propanal, 2,2-bis(phenylthio)-(77331-03-4)

Safety Data

• Hazardous Substances Data: 77331-03-4(Hazardous Substances Data)

Upstream product

• 27313-32-2 2,2-dichloropropanal 
• 13133-62-5 thiophenolate 
• 930-69-8 sodium thiophenolate 
• 102-69-2 tri-n-propylamine 
• 108-98-5 thiophenol 
• 55064-96-5 2-(phenylthio)propanal 
• 77331-00-1 2-Chloro-2-phenylsulfanyl-propionaldehyde 

Relevant articles and documents

Synthesis of α,α-Disulfenylated Aldehydes via Oxidative Transformation of Tertiary Amines

A method for the copper-catalyzed regioselective β-functionalization of tertiary amines with thiophenols has been developed. The control experiments and primary studies show that a thiyl radical is involved in the reaction, and the method provides a novel

Allylation with substituted vinylthionium ions from SnCl4 ionisation of 1,3- and 3,3-bis(alkyl/phenylthio)propenes

α- and γ-substituted vinylthionium ions from SnCl4 ionisation of a range of substituted 1,3- and 3,3-bis(alkyl/phenylthio)propenes allylate enol silyl ethers in good yield. Levels of regioselectivity are sterically dependent and in the case of

α-CETOALDEHYDES A GROUPEMENT ALDEHYDIQUE OU CETONIQUE PROTEGE

α-Ketoaldehydes with protected ketogroup 2 or protected aldehydrogroup 3 are obtained by reaction of thiophenol or methanol with α-chloro-α-(phenylthio)aldehydes 7.