1334172-22-3

Basic information

• Product Name: S-phenyl 3-(phenylsulfanyl)-3-p-tolylpropanethioate
• Synonyms: S-phenyl 3-(phenylsulfanyl)-3-p-tolylpropanethioate
• CAS NO: 1334172-22-3
• Molecular Weight: 364.532
• Mol File: 1334172-22-3.mol

Chemical Properties

• CAS DataBase Reference: S-phenyl 3-(phenylsulfanyl)-3-p-tolylpropanethioate(CAS DataBase Reference)
• NIST Chemistry Reference: S-phenyl 3-(phenylsulfanyl)-3-p-tolylpropanethioate(1334172-22-3)
• EPA Substance Registry System: S-phenyl 3-(phenylsulfanyl)-3-p-tolylpropanethioate(1334172-22-3)

Safety Data

• Hazardous Substances Data: 1334172-22-3(Hazardous Substances Data)

Upstream product

• 1504-75-2 3-(4-methylphenyl)acrylaldehyde 
• 882-33-7 diphenyldisulfane 
• 104-87-0 4-methyl-benzaldehyde 
• 1866-39-3 trans-p-methylcinnamic acid 
• 1334172-14-3 1-(1H-1,2,3-benzotriazol-1-yl)-3-(phenylthio)-3-p-tolylpropan-1-one 
• 108-98-5 thiophenol 
• 881901-86-6 (E)-1-(benzotriazol-1-yl)-3-(4-methylphenyl)-2-propen-1-one 

Relevant articles and documents

Unprecedented dithiolation of enals via their NHC-catalysed umpolung reaction with organic disulfides

A novel one-pot N-heterocyclic carbene (NHC)-catalysed dithiolation of α,β-unsaturated aldehydes (enals) with organic disulfides is reported. The protocol involves homoenolate reactivity of enals, where the homoenolate attacks on the disulfide as a d

Regioselective addition of thiophenol to α,β-unsaturated N-acylbenzotriazoles

Regioselective addition of thiophenol to α,β-unsaturated N-acylbenzotriazoles has been achieved by controlling the conditions. Thus, three types of products, namely α,β-unsaturated thioesters, β-thiophenoxy substituted N-acylbenzotriazoles, and β-thiophenoxy substituted thioesters were selectively obtained in good to excellent yields.