155237-72-2

Basic information

• Product Name: (1R,2R)-N,N'-bis-(p-nitrobenzenesulfonyl)-1,2-cyclohexanediamine
• Synonyms: (1R,2R)-N,N'-bis-(p-nitrobenzenesulfonyl)-1,2-cyclohexanediamine
• CAS NO: 155237-72-2
• Molecular Weight: 484.511
• Mol File: 155237-72-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (1R,2R)-N,N'-bis-(p-nitrobenzenesulfonyl)-1,2-cyclohexanediamine(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2R)-N,N'-bis-(p-nitrobenzenesulfonyl)-1,2-cyclohexanediamine(155237-72-2)
• EPA Substance Registry System: (1R,2R)-N,N'-bis-(p-nitrobenzenesulfonyl)-1,2-cyclohexanediamine(155237-72-2)

Safety Data

• Hazardous Substances Data: 155237-72-2(Hazardous Substances Data)

Upstream product

• 138-42-1 p-nitrobenzenesulfonic acid 
• 20439-47-8 (1R,2R)-1,2-diaminocyclohexane 
• 98-74-8 4-Nitrobenzenesulfonyl chloride 

Relevant articles and documents

MgBr2-promoted enantioselectIVe aryl addition of ArTi(OiPr)3 to ketones catalyzed by a titanium(IV) catalyst of N,N′-sulfonylated (1R,2R)-cyclohexane-1,2-diamine

MgBr2-promoted asymmetric addition of ArTi(OiPr)3 to ketones catalyzed by a titanium catalyst of N,N′-sulfonylated (1R,2R)-cyclohexane-1,2-diamines is reported, and results showed that the chiral N,N′-sulfonylated cyclohex

A Catalytic Enantioselective Reaction Using a C2-Symmetric Disulfonamide as a Chiral Ligand: Simmons-Smith Cyclopropanation of Allylic Alcohols by the Et2Zn-CH2I2-Disulfonamide System

A catalytic and enantioselective Simmons-Smith cyclopropanation of an allylic alcohol was developed by the reaction of an allylic alcohol with Et2Zn and CH2I2 in the presence of a catalytic amount of chiral disulfonamide 4.