32363-23-8

Basic information

• Product Name: 6,6-dimethylcyclohex-1-en-1-yl trifluoromethanesulfonate
• Synonyms: 6,6-dimethylcyclohex-1-en-1-yl trifluoromethanesulfonate
• CAS NO: 32363-23-8
• Molecular Weight: 258.262
• Mol File: 32363-23-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 6,6-dimethylcyclohex-1-en-1-yl trifluoromethanesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 6,6-dimethylcyclohex-1-en-1-yl trifluoromethanesulfonate(32363-23-8)
• EPA Substance Registry System: 6,6-dimethylcyclohex-1-en-1-yl trifluoromethanesulfonate(32363-23-8)

Safety Data

• Hazardous Substances Data: 32363-23-8(Hazardous Substances Data)

Upstream product

• 37595-74-7 N,N-phenylbistrifluoromethane-sulfonimide 
• 1193-47-1 2,2-dimethyl-cyclohexanone 
• 145100-51-2 N-(5-chloropyridin-2-yl)-1,1,1-trifluoro-N-[(trifluoromethyl)sulphonyl]methanesulphonamide 

Downstream Products

• 1142225-97-5 2-(6,6-dimethyl-1-cyclohexen-1-yI)-4,4,5,5-tetramethyI-1,3,2-dioxaborolane 
• 1254470-32-0 1,2,3,4-tetrahydro-2-(3-(6,6-dimethylcyclohex-1-enyl)-1-phenylprop-2-ynyl)isoquinoline 
• 1393654-57-3 3-(3-(6,6-dimethylcyclohex-1-en-1-yl)propyl)-2H-chromen-2-one 
• 309718-50-1 tert-butyl 2-[(6,6-dimethylcyclohex-1-enyl)carbonyl]indole-1-carboxylate 
• 105593-28-0 β-ionone 
• 167102-41-2 (6,6-Dimethyl-cyclohex-1-enyl)-(1-methyl-1H-indol-2-yl)-methanone 
• 1142226-06-9 (2-(2,2-dimethylcyclohexyl)-2'-fluoro-5'-(methyloxy)-1,1'-biphenyl-4-yl)methanol 

Relevant articles and documents

Catalytic allylic oxidation to generate vinylogous acyl sulfonates from vinyl sulfonates

Regioselective formation of vinylogous acyl sulfonates was accomplished via the allylic oxidation of the corresponding vinyl sulfonates. The reaction progressed through the agency of catalytic iron(III) chloride catalysis with tert-Butyl hydroperoxide (TBHP) as the stoichiometric oxidant. Tolerance of other functional groups, including some other allylic and benzylic sites, was observed.

INHIBITORS OF VIRAL REPLICATION, THEIR PROCESS OF PREPARATION AND THEIR THERAPEUTICAL USES

The present invention relates to compounds of formula (1) as claimed in claim 1, their use in the treatment or the prevention of viral disorders, including HIV. (Formula I)

INDANYLOXYDIHYDROBENZOFURANYLACETIC ACIDS

The present invention relates to compounds defined by formula (I) wherein the variables R1, R2, R3, m, and n are defined as in claim 1, possessing valuable pharmacological activity. Particularly, the compounds are activators of the receptor GPR40 and thus are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular diabetes type 2.