91146-10-0

Basic information

• Product Name: cis-1,2-cyclohexanediyl 1,2-bis(trifluoromethanesulfonate)
• Synonyms: cis-1,2-cyclohexanediyl 1,2-bis(trifluoromethanesulfonate)
• CAS NO: 91146-10-0
• Molecular Weight: 380.286
• Mol File: 91146-10-0.mol

Chemical Properties

• CAS DataBase Reference: cis-1,2-cyclohexanediyl 1,2-bis(trifluoromethanesulfonate)(CAS DataBase Reference)
• NIST Chemistry Reference: cis-1,2-cyclohexanediyl 1,2-bis(trifluoromethanesulfonate)(91146-10-0)
• EPA Substance Registry System: cis-1,2-cyclohexanediyl 1,2-bis(trifluoromethanesulfonate)(91146-10-0)

Safety Data

• Hazardous Substances Data: 91146-10-0(Hazardous Substances Data)

Upstream product

• 75-05-8 acetonitrile 
• 110-83-8 cyclohexene 
• 358-23-6 trifluoromethylsulfonic anhydride 
• 536-80-1 iodosylbenzene 
• 71-43-2 benzene 
• 1493-13-6 trifluorormethanesulfonic acid 
• 88016-29-9 μ-oxobis[(trifluoromethanesulfonato)(phenyl)iodine] 
• 108-88-3 toluene 
• 108-90-7 chlorobenzene 
• 100-66-3 methoxybenzene 
• 140-29-4 phenylacetonitrile 
• 123-02-4 tridecylbenzene 
• 496-11-7 INDANE 
• 106-42-3 para-xylene 

Relevant articles and documents

Reactions of [fluoro(methylsulfonyloxy)iodo]benzene: I. Reaction of [fluoro(sulfonyloxy)iodo]benzene with monocyclic olefins

Reactions of [fluoro(methylsulfonyloxy)iodo]benzene and [fluoro(trifluoromethylsulfonyloxy)-iodo]benzene with cyclohexene, cyclopentene, and cyclopentadiene in the presence and absence of external nucleophiles were studied.

Preparation of (p-Phenylene)bis(aryliodonium) Ditriflates and Their Double Substitution by Some Nucleophiles

A reagent prepared from a 1:1 molar mixture of PhIO and Tf2O or from a 1:2 molar mixture of PhIO and TfOH shows high reactivity towards aromatic substrates and gives (p-phenylene)bis(aryliodonium) ditriflates (8).Interaction of the reagent wit

NOVEL REAGENTS CONTAINING HYPERVALENT IODINE AND THEIR USE FOR ELECTROPHILIC ADDITIONS TO OLEFINS

A series of novel I(III) containing reagents have been developed and their electrophilic reactions with olefins giving vic-disubstituted derivatives (including vic-ditriflates) are described.