67808-91-7

Upstream product

• 67808-90-6 1-nitro-1-(phenylthio)-2-propanol 
• 60595-16-6 (phenylthio)nitromethane 
• 75-07-0 acetaldehyde 

Downstream Products

• 67808-97-3 3,6-Dimethyl-2-phenylsulfanyl-6,7-dihydro-5H-benzofuran-4-one 
• 73805-34-2 (Z)-2-(phenylthio)-3-methyl-4-oxo-6-methyl-2,3,4,5,6,7-hexahydrobenzofuran 
• 73805-33-1 (E)-2-(phenylthio)-3-methyl-4-oxo-6-methyl-2,3,4,5,6,7-hexahydrobenzofuran 
• 96746-22-4 C₁₇H₁₃N₂O₄S^(1-)*K⁽¹⁺⁾ 
• 78924-46-6 3,6-Dimethyl-2-phenylsulfanyl-6-vinyl-3,5,6,7-tetrahydro-2H-benzofuran-4-one 
• 109975-72-6 N-<1-<(phenylthio)carbonyl>ethyl>-4-phenyl-2-azetidinone 
• 114805-68-4 3-Methyl-2-nitro-2-phenylthio Oxirane 
• 92339-67-8 S-phenyl 2-methoxy(thiopropanoate) 
• 92339-69-0 S-phenyl 2-phthalimido(thiopropanoate) 
• 92339-68-9 S-phenyl 2-isopropoxy(thiopropanoate) 
• 92339-70-3 S-phenyl 2-(fluoracetamido)thiopropanoate 
• 92339-72-5 methyl 2-(methoxycarbonyl)-3-<(phenylthio)carbonyl>butanoate 
• 92339-71-4 S-phenyl 2-(toluene-4-sulfonyl)thiopropanoate 
• 132364-65-9 S-Phenyl 2-Fluoro(thiopropanoate) 

Relevant academic research and scientific papers

Preparation and Synthetic Utility of 1-Phenylthio-1-nitro Epoxides. Facile Preparation of α-Substituted S-Phenyl Thio esters

Novel 1-Phenylthio-1-nitro epoxides (2), readily prepared by epoxidation of the corresponding 1-phenylthio-1-nitroalkenes (1), react efficiently under mild conditions with a variety with a variety of hetero nucleophiles to give α-substituted S-phenyl thio

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

(Phenylthio)nitromethane: A Convenient Reagent for the Construction of Bicyclic β-Lactams

2--1-azabicyclooctan-8-one (10), 2-1-1-azabicycloheptan-7-one (12), and 3,3-dimethyl-2--4-oxa-1-azabicycloheptan-7-one were prepared in high overall yields from monocyc

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

1-Nitro-1-(phenylthio)propene as a New Nitro Olefin Reagent for 3-Methylfuran Annulation and Its Application to the Synthesis of Some Furanoterpenoids

1-Nitro-1-(phenylthio)propene (9) was synthesized from (phenylthio)acetic acid (6) in five steps.This nitro olefin reacted with dimedone (1) with KF catalysis to yield dihydrofurans 10a and 10b, both of which were converted to 3-methylfuran 13 on NaIO4 ox