96746-22-4

Basic information

• Product Name: C₁₇H₁₃N₂O₄S^(1-)*K⁽¹⁺⁾
• Synonyms: C₁₇H₁₃N₂O₄S^(1-)*K⁽¹⁺⁾
• CAS NO: 96746-22-4
• Molecular Weight: 380.466
• Mol File: 96746-22-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: C₁₇H₁₃N₂O₄S^(1-)*K⁽¹⁺⁾(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₇H₁₃N₂O₄S^(1-)*K⁽¹⁺⁾(96746-22-4)
• EPA Substance Registry System: C₁₇H₁₃N₂O₄S^(1-)*K⁽¹⁺⁾(96746-22-4)

Safety Data

• Hazardous Substances Data: 96746-22-4(Hazardous Substances Data)

Upstream product

• 67808-90-6 1-nitro-1-(phenylthio)-2-propanol 
• 67808-91-7 (Z)-1-nitro-1-(phenylthio)propene 
• 1074-82-4 potassium phtalimide 
• 60595-16-6 (phenylthio)nitromethane 

Downstream Products

• 92339-69-0 S-phenyl 2-phthalimido(thiopropanoate) 

Relevant articles and documents

Preparation of α-Substituted S-Phenyl Thio Esters from Aldehydes and (Phenylthio)nitromethane

Acetaldehyde and isobutyraldehyde, RCHO, reacted with (phenylthio)nitromethane (KO-t-Bu, THF, t-BuOH) followed by methanesulfonyl chloride (Et3N, CH2Cl2) to give the (Z)-alkenes RCH=C(SPh)NO2.These reacted with the nucleophiles NuM = potassium phthalimid

Phenylthionitromethane: a Versatile Reagent for the Conversion of Aldehydes into α-Substituted S-Phenyl Thioesters

Acetaldehyde and isobutyraldehyde, RCHO, reacted with phenylthionitromethane (KOH, MeOH) followed by methanesulphonyl chloride (Et3N, CH2Cl2) to give the alkenes, RCH=C(SPh)NO2; these reacted with the nucleophiles i, potassium