5700-44-7

Basic information

• Product Name: Benzene,(1-cyclohexylethenyl)-
• CAS NO: 5700-44-7
• Molecular Weight: 186.297
• Mol File: 5700-44-7.mol
• Article Data: 32

Chemical Properties

• CAS DataBase Reference: Benzene,(1-cyclohexylethenyl)- (CAS DataBase Reference)
• NIST Chemistry Reference: Benzene,(1-cyclohexylethenyl)- (5700-44-7)
• EPA Substance Registry System: Benzene,(1-cyclohexylethenyl)- (5700-44-7)

Safety Data

• Hazardous Substances Data: 5700-44-7(Hazardous Substances Data)

Upstream product

• 712-50-5 Cyclohexyl phenyl ketone 
• 14399-53-2 bis(iodomethyl)zinc 
• 100-52-7 benzaldehyde 
• 695-12-5 vinylcyclohexane 
• 640-60-8 toluene-4-sulfonic acid phenyl ester 
• 16156-59-5 phenyl methanesulfonate 
• 17763-67-6 Phenyl triflate 
• 67300-99-6 1-phenylethenylmagnesium bromide 
• 931-50-0 cyclohexylmagnesium bromide 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 4922-43-4 dodecyl 1-phenylethenyl sulfide 
• 5664-20-0 vinylidenecyclohexane 
• 591-50-4 iodobenzene 
• 2043-61-0 cyclohexanecarbaldehyde 

Downstream Products

• 46498-49-1 3-Cyclohexyl-3-phenylpropanal 
• 91704-75-5 (R)-(+)-1-cyclohexyl-1-phenyl-ethane-1,2-diol 
• 61153-38-6 (E)-1-(2-cyclohexylvinyl)-4-methylbenzene 
• 91704-75-5 (S)-(-)-1-cyclohexyl-1-phenyl-1,2-etanediol 
• 4413-16-5 1-ethyl-4-phenylcyclohexane 
• 55983-32-9 2-methyl-2-phenylmethylenecyclohexane 
• 4361-40-4 3-cyclohexyl-3-phenylpropanoic acid 
• 75-89-8 2,2,2-trifluoroethanol 
• 75-90-1 2,2,2-Trifluoroacetaldehyde 
• 712-50-5 Cyclohexyl phenyl ketone 

Relevant articles and documents

Electrochemical fluorosulfonylation of alkenes to access vicinal fluorinated sulfones derivatives

Herein, we report a practical and efficient fluorosulfonylation of the various alkenes with sulfonyl radical sources (RSO2NHNH2) and Et3N·3HF as cost-effective fluorination reagents under mild conditions. Remarkably, this

Photoinduced Hydroarylation and Cyclization of Alkenes with Luminescent Platinum(II) Complexes

Photoinduced hydroarylation of alkenes is an appealing synthetic strategy for arene functionalization. Herein, we demonstrated that aryl radicals generated from electron-deficient aryl chlorides/bromides could be trapped by an array of terminal/internal aryl alkenes in the presence of [Pt(O^N^C^N)] under visible-light (410 nm) irradiation, affording anti-Markovnikov hydroarylated compounds in up to 95 % yield. Besides, a protocol for [Pt(O^N^C^N)]-catalyzed intramolecular photocyclization of acrylanilides to give structurally diverse 3,4-dihydroquinolinones has been developed.

Electrochemical fluorosulfonylation of styrenes

An environmentally friendly and efficient electrochemical fluorosulfonylation of styrenes has been developed. With the use of sulfonylhydrazides and triethylamine trihydrofluoride, a diverse array of β-fluorosulfones could be readily obtained. This reaction features mild conditions and a broad substrate scope, which could also be conveniently extended to a gram-scale preparation.