86029-83-6

Basic information

• Product Name: 2-(2-phenyl-1-ethenyl)cyclohexanone
• Synonyms: 2-(2-phenyl-1-ethenyl)cyclohexanone
• CAS NO: 86029-83-6
• Molecular Weight: 200.28
• Mol File: 86029-83-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-(2-phenyl-1-ethenyl)cyclohexanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-phenyl-1-ethenyl)cyclohexanone(86029-83-6)
• EPA Substance Registry System: 2-(2-phenyl-1-ethenyl)cyclohexanone(86029-83-6)

Safety Data

• Hazardous Substances Data: 86029-83-6(Hazardous Substances Data)

Upstream product

• 108-94-1 cyclohexanone 
• 536-74-3 phenylacetylene 
• 82202-15-1 2-<(phenylthio)trimethylsilylmethyl>cyclohexanone 
• 79239-13-7 trimethylsilane 
• 86029-74-5 bromphenylthiotrimethylsilylmethane 
• 17873-08-4 (phenylsulfanylmethyl)trimethylsilane 
• 6651-36-1 1-(Trimethylsilyloxy)cyclohexene 
• 86029-81-4 [(1,4-Dioxa-spiro[4.5]dec-6-yl)-phenylsulfanyl-methyl]-trimethyl-silane 
• 100-52-7 benzaldehyde 

Downstream Products

• 2305-85-3 5,6,7,8-tetrahydroquinazolin-2-amine 

Relevant articles and documents

2-Aminopyrimidines in just two steps from ketones, acetylenes and guanidine via β,γ enones

Available β,γ-enones, the products of nucleophilic addition of ketones to phenylacetylene, react with guanidine in the KOH / DMSO system at 70?°C to give 2-aminopyrimidines in up to 72% yield.

Transition-metal-catalyzed rearrangement of 1,1-(Oligomethylene)-4-aryl-2- butene-1,4-diols: Ring expansion vs. aryl group migration

The transition-metal-catalyzed rearrangement of 1,1-(oligomethylene)-4- aryl-2-butene-1,4-diols was investigated. In the presence of PdCl 2(MeCN)2 and Cu(OTf)2, a rapidly equilibrating 1,3-isomerization is followed by 1,2-

PROCESS FOR THE PREPARATION OF ORGANIC COMPOUNDS WITH MANGANESE CATALYSTS OR THE LIKE

A process of the present invention produces an organic compound by allowing a compound containing an electron attractive group of following Formula (1):wherein Y is an electron attractive group; and Rb and Rc are each a hydrogen atom or an organic group, where Y, Rb and Rc may respectively be combined with each other to form a ring with an adjacent carbon atom, to react with a compound containing an unsaturated carbon-carbon bond of following Formula (2) or (7):wherein Rd, Re, Rf, Rg, Ri and Rj are each a hydrogen atom or an organic group, where Rd, Re, Rf and Rg may respectively be combined to form a ring with one or two adjacent carbon atoms, and Ri and Rj may be combined to form a ring with adjacent two carbon atoms, in the presence of oxygen and a catalytic compound of a Group 5, 6, 7, 8 or 9 element of the Periodic Table of Elements to yield a compound of following Formula (3) or (8):wherein Z is a hydrogen atom or a hydroxyl group; and Y, Rb, Rc, Rd, Re, Rf, Rg, Ri and Rj have the same meanings as defined above. This process can efficiently produce a compound having an alkyl group or alkenyl group bonded at the alpha position of an electron attractive group, or a derivative thereof, by catalytic radical addition reaction.