28215-02-3

Basic information

• Product Name: Disulfide, 2-nitrophenyl phenyl
• CAS NO: 28215-02-3
• Molecular Formula: C12H9NO2S2
• Molecular Weight: 263.341
• Mol File: 28215-02-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Disulfide, 2-nitrophenyl phenyl(CAS DataBase Reference)
• NIST Chemistry Reference: Disulfide, 2-nitrophenyl phenyl(28215-02-3)
• EPA Substance Registry System: Disulfide, 2-nitrophenyl phenyl(28215-02-3)

Safety Data

• Hazardous Substances Data: 28215-02-3(Hazardous Substances Data)

Upstream product

• 108-98-5 thiophenol 
• 53888-05-4 1-(2-nitro-phenylsulfanyl)-indole-2,3-dione 
• 28833-58-1 C₂₄H₂₀N₂O₄S₄ 
• 22755-25-5 o-nitrobenzenethiol sodium salt 
• 4875-10-9 o-nitrothiophenol 
• 1155-00-6 bis(2-nitrophenyl)disulfide 
• 882-33-7 diphenyldisulfane 
• 28074-23-9 phenylsulfenyl bromide 
• 14933-91-6 N-phenyl-benzenesulphenamide 
• 884-09-3 phenyl thiobenzoate 
• 22024-99-3 2-nitrobenzenesulfenyl bromide 
• 7257-62-7 4-[(2-nitrophenyl)sulfanyl]morpholine 
• 78945-05-8 S-phenyl pent-4-enethioate 
• 29572-51-8 2-nitrobenzenesulfenyl thiocyanate 

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 
• 882-33-7 diphenyldisulfane 
• 125904-72-5 mercury o-nitrophenyl mercaptide 
• 18112-86-2 N¹,N²-Bis--benzolsulfinsaeureamidin 
• 983-79-9 benzophenone azine 
• 20834-65-5 (2,4-dinitro-phenyl)-(2-nitro-phenyl)-sulfide 
• 4875-10-9 o-nitrothiophenol 

Relevant articles and documents

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.

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

Behaviours of N (substituted thio)phthalimides, N (substituted thio)succinimides, and N (substituted thio)isatins toward some nucleophiles

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