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 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 67300-99-6 1-phenylethenylmagnesium bromide 
• 931-50-0 cyclohexylmagnesium bromide 
• 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 
• 4922-43-4 dodecyl 1-phenylethenyl sulfide 
• 5664-20-0 vinylidenecyclohexane 
• 591-50-4 iodobenzene 
• 2043-61-0 cyclohexanecarbaldehyde 

Downstream Products

• 55983-32-9 2-methyl-2-phenylmethylenecyclohexane 
• 4413-16-5 1-ethyl-4-phenylcyclohexane 
• 91704-75-5 (R)-(+)-1-cyclohexyl-1-phenyl-ethane-1,2-diol 
• 144313-98-4 2-cyclohexyl-2-phenyloxirane 
• 5664-22-2 (+/-)-2-cyclohexyl-2-phenylacetaldehyde 
• 46498-49-1 3-Cyclohexyl-3-phenylpropanal 
• 91704-75-5 (S)-(-)-1-cyclohexyl-1-phenyl-1,2-etanediol 
• 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 
• 31378-03-7 1-phenyl-2-tosylethanone 
• 40240-72-0 (E)-1-(4-methoxyphenyl)-4-phenylbut-2-ene-1,4- dione 

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 [3+2] Annulation of Alkene with o-Iodoanilines: An Expedient Approach to Indolines

A highly regioselective [3+2] cyclization of alkenes with 2-iodoanilines under the irradiation of UV light is described. This general, metal-free strategy facilitates the direct preparation of 2-mono-/disubstituted indolines as well as spiroindolines through alkene carboamination in one step. Mechanistic studies suggested that the photochemical protocol proceeded via a radical pathway.

Visible-Light-Induced Meerwein Fluoroarylation of Styrenes

An unprecedented approach for assembling a broad range of 1,2-diarylethane derivatives with fluorine-containing fully substituted carbon centers was developed. The protocol features straightforward operation, proceeds under metal-free condition, and accommodates a large variety of synthetically useful functionalities. The critical aspect to the success of this novel transformation lies in using aryldiazonium salts as both aryl radical progenitor and also as single electron acceptor which elegantly enables a radical-polar crossover manifold.