28215-02-3

Upstream product

• 60-29-7 diethyl ether 
• 7669-54-7 2-nitrobenzenesulfenyl chloride 
• 108-98-5 thiophenol 
• 2769-30-4 2-nitrophenyl thiocyanate 
• 29572-51-8 2-nitrobenzenesulfenyl thiocyanate 
• 71-43-2 benzene 
• 53888-05-4 1-(2-nitro-phenylsulfanyl)-indole-2,3-dione 
• 7257-62-7 4-[(2-nitrophenyl)sulfanyl]morpholine 
• 78945-05-8 S-phenyl pent-4-enethioate 
• 28833-58-1 C₂₄H₂₀N₂O₄S₄ 
• 22755-25-5 o-nitrobenzenethiol sodium salt 
• 884-09-3 phenyl thiobenzoate 
• 1155-00-6 bis(2-nitrophenyl)disulfide 
• 882-33-7 diphenyldisulfane 

Downstream Products

• 1155-00-6 bis(2-nitrophenyl)disulfide 
• 18512-80-6 benzenethiosulfonic acid S-(2-nitro-phenyl ester) 
• 1212-08-4 S-Phenyl benzenethiosulfonate 
• 7669-57-0 S-(2-nitrophenyl) 2-nitrobenzene thiosulfonate 
• 4875-10-9 o-nitrothiophenol 
• 882-33-7 diphenyldisulfane 
• 20834-65-5 (2,4-dinitro-phenyl)-(2-nitro-phenyl)-sulfide 
• 983-79-9 benzophenone azine 
• 18112-86-2 N¹,N²-Bis--benzolsulfinsaeureamidin 
• 125904-72-5 mercury o-nitrophenyl mercaptide 

Relevant academic research and scientific papers

NFSI-catalyzed S[sbnd]S bond exchange reaction for the synthesis of unsymmetrical disulfides

The metal-free S[sbnd]S bond exchange reaction of symmetrical disulfides catalyzed by NFSI is described. This novel protocol provides a facile and efficient approach to accessing important unsymmetrical disulfides. Furthermore, this strategy could also be utilized in the late-stage functionalization of amino acids, drugs, and natural products. The broad substrate scope, good functional group tolerance and easy accessibility of catalyst indicate that this strategy affords a green and practical complementary method to various unsymmetrical disulfides.

Imination of sulfur-containing compounds: XXXV. New preparation method and oxidative benzenesulfonylimination of unsymmetrical disulfides

A new preparative method of synthesis was developed for unsymmetrical and symmetrical disulfides. This method involves sulfenylation of sodium thiolates with N-arenesulfenyl-N,N′-bis(arenesulfonyl)sulfinamidines. Imination of unsymmetrical disulfides with sodium chloroamides of sulfonic acids occurs at the more nucleophilic sulfur atom, affording N,N′ -bis(arenesulfonyl)sulfinamidines and symmetrical disulfides.

Ortho Effects in Organic Molecules on Electron Impact: 21 - Oxygen Transfers from the Ortho Nitro Group to Sulphur in N-Aryl-2-nitrobenzenesulphenamides and Phenyl-2-nitrophenyl Disulphide

Fragment ions arising as a result of oxygen transfer from the nito group to sulphur have been noticed in N-aryl-2-nitrobenzenesulphenamides and phenyl-2-nitrophenyl disulphide.In the case of the former a double oxygen transfer to the sulphur has been noti