1374869-65-4

Basic information

• Product Name: N,N'-(1-cyclohexylethane-1,2-diyl)bis(4-methyl-N-tosylbenzenesulfonamide)
• Synonyms: N,N'-(1-cyclohexylethane-1,2-diyl)bis(4-methyl-N-tosylbenzenesulfonamide)
• CAS NO: 1374869-65-4
• Molecular Weight: 759.002
• Mol File: 1374869-65-4.mol

Chemical Properties

• CAS DataBase Reference: N,N'-(1-cyclohexylethane-1,2-diyl)bis(4-methyl-N-tosylbenzenesulfonamide)(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-(1-cyclohexylethane-1,2-diyl)bis(4-methyl-N-tosylbenzenesulfonamide)(1374869-65-4)
• EPA Substance Registry System: N,N'-(1-cyclohexylethane-1,2-diyl)bis(4-methyl-N-tosylbenzenesulfonamide)(1374869-65-4)

Safety Data

• Hazardous Substances Data: 1374869-65-4(Hazardous Substances Data)

Upstream product

• 695-12-5 vinylcyclohexane 
• 3695-00-9 di(4-tosyl)amine 

Relevant articles and documents

Iodine(III)-promoted intermolecular diamination of alkenes

A rapid and productive vicinal diamination of alkenes takes place in the presence of a hypervalent iodine(III) reagent and bissulfonimides as nitrogen sources. A total of more than 60 examples are presented. The reaction is characterized by its robustness and its wide substrate scope: it proceeds selectively with both terminal and internal alkenes and tolerates a range of functional groups.

NOVEL IODINE COMPOUNDS, PROCESSES FOR THEIR PREPARATION AND USE THEREOF AS AMINATION AGENTS

The iodine compounds of the present invention corresponds to those of formula (I), wherein R1, R1' and X have several meanings. These iodine compounds gives rise to the amination of several substrates without the need of catalysts, especially metal catalysts, and confer to the amination reaction the further advantage of being performed under mild conditions, which is of interest for industrial-scale production of nitrogenated compounds with pharmaceutical, biological or medicinal applications. Therefore, the iodine compounds of the invention are useful as amination agents. The invention also discloses several processes for the preparation of the iodine compounds of formula (I).