131665-81-1

Basic information

• Product Name: 3-cyclohexylprop-2-enyl bromide
• Synonyms: 3-cyclohexylprop-2-enyl bromide
• CAS NO: 131665-81-1
• Molecular Weight: 203.122
• Mol File: 131665-81-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-cyclohexylprop-2-enyl bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-cyclohexylprop-2-enyl bromide(131665-81-1)
• EPA Substance Registry System: 3-cyclohexylprop-2-enyl bromide(131665-81-1)

Safety Data

• Hazardous Substances Data: 131665-81-1(Hazardous Substances Data)

Upstream product

• 695-12-5 vinylcyclohexane 
• 106-95-6 allyl bromide 
• 37868-74-9 3-cyclohexyl-2-propenal 
• 6048-09-5 3-cyclohexylacrylic acid ethyl ester 
• 2043-61-0 cyclohexanecarbaldehyde 
• 4352-44-7 1-cyclohexylprop-2-en-1-ol 
• 42134-55-4 3-cyclohexyl-2-propen-1-ol 

Downstream Products

• 1214913-17-3 (E)-(3-cyclohexylallyl)dimethyl(phenyl)silane 
• 1542395-36-7 (1-azidoallyl)cyclohexane 
• 1265145-55-8 (+)-(R)-3-cyclohexyl-3-(4-fluorophenyl)prop-1-ene 
• 169524-62-3 C₁₆H₂₂ 
• 1265145-53-6 (+)-(R)-3-cyclohexyl-3-(4-tolyl)prop-1-ene 
• 847610-46-2 (-)-(S)-3-cyclohexyl-3-phenylprop-1-ene 
• 137542-88-2 (+)-(R)-3-cyclohexyl-3-phenylpropan-1-ol 
• 1265145-54-7 (+)-(R)-3-(4-chlorophenyl)-3-cyclohexylprop-1-ene 
• 1265145-57-0 (+)-(R)-3-cyclohexyl-3-(3,4-methylenedioxyphenyl)prop-1-ene 
• 1265145-56-9 (+)-(R)-3-cyclohexyl-3-(3,4-dichlorophenyl)prop-1-ene 

Relevant articles and documents

Highly selective hydrosilylation of equilibrating allylic azides

The Pt-catalyzed hydrosilylation of equilibrating allylic azides is reported. The reaction provides only one out of four possible hydrosilylation products in good yields and with very high chemoselectivity (alk-1-enevs.alk-2-ene), regioselectivity (linearvs.branched), and excellent functional group tolerance.

Copper-catalyzed vinylsilane allylation

Soft reaction conditions, particularly important in total synthesis, have dragged many researchers into the field of silylated organic compounds. Hereby, we describe a new copper-catalyzed vinylsilane transformation. Various vinylsilanes were allylated by using a copper(I) salt, and this led to the formation of polysubstituted 1,4-dienes bearing sensitive moieties such as halogens, ketones, and aldehydes. Hereby is described a new copper-catalyzed vinylsilane transformation. Various vinylsilanes were allylated by using copper(I) salts, and this led to the formation of polysubstituted 1,4-dienes bearing sensitive moieties such as halogens, ketones, and aldehydes. TBAT = tetrabutylammonium difluorotriphenylsilicate. Copyright

Negative inotropic and calcium antagonistic activity of alkyl and arylalkyl phosphonates

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