1150-28-3

Basic information

• Product Name: Benzenesulfonothioic acid, S-(4-nitrophenyl) ester
• CAS NO: 1150-28-3
• Molecular Formula: C12H9NO4S2
• Molecular Weight: 295.34
• Mol File: 1150-28-3.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Benzenesulfonothioic acid, S-(4-nitrophenyl) ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonothioic acid, S-(4-nitrophenyl) ester(1150-28-3)
• EPA Substance Registry System: Benzenesulfonothioic acid, S-(4-nitrophenyl) ester(1150-28-3)

Safety Data

• Hazardous Substances Data: 1150-28-3(Hazardous Substances Data)

Upstream product

• 873-55-2 sodium benzenesulfonate 
• 1849-36-1 para-nitrobenzenethiol 
• 80-17-1 benzenesufonyl hydrazide 
• 100-32-3 di(p-nitrophenyl) disulfide 
• 24308-84-7 zinc benzenesulfinate 
• 16599-39-6 benzenethiosulfonic acid ; potassium-salt 
• 100-01-6 4-nitro-aniline 
• 91363-26-7 p-nitrophenylazobenzenethiosulfonate 
• 84452-55-1 N-4-nitrophenylthio-1,4-benzoquonone imine 

Downstream Products

• 1227258-22-1 1-hexyl p-nitrophenyl disulfide 
• 22873-15-0 N-(methyl)carbamate du nitro-4 thiophenol 
• 7305-12-6 S-(p-nitrophenyl) N,N-dimethylthiocarbamate 
• 17041-81-5 p-tolyl benzenethiosulfonate 
• 112128-60-6 N,N-Diethyl-S-(4-nitro-phenyl)-thiohydroxylamine 
• 1212-08-4 S-Phenyl benzenethiosulfonate 

Relevant articles and documents

Visible-light-promoted synthesis of secondary and tertiary thiocarbamates from thiosulfonates andN-substituted formamides

A general visible-light-promoted metal-free synthesis of secondary and tertiary thiocarbamates starting from thiosulfonates andN-substituted formamides is developed. By employing rhodamine B as a photocatalyst andtert-butyl hydroperoxide (TBHP) as an oxidant, a wide scope of thiocarbamates can be obtained through direct thiolation of acyl C-H bonds under irradiation of blue light at room temperature for 12 h.

Gold/photoredox-cocatalyzed atom transfer thiosulfonylation of alkynes: Stereoselective synthesis of vinylsulfones

We report a gold and photoredox combined radical approach for the rapid synthesis of thio-functionalized vinylsulfones from alkynes. Key features of this method include very mild conditions, broad substrate scope, excellent regio- and stereoselectivties, and 100% atom economy.

Visible-light-induced thiotrifluoromethylation of terminal alkenes with sodium triflinate and benzenesulfonothioates

An unconventional reductive quenching cycle was developed to realize the visible-light-induced thiotrifluoromethylation of terminal alkenes. CF3SO2Na was used as an easy to handle CF3 radical source to afford the desired products in moderate to good yields. Mild reaction conditions and a broad substrate scope feature in this transformation.