29179-20-2

Basic information

• Product Name: 2-Cyclohexen-1-one, 3-(2-phenylethenyl)-, (E)-
• CAS NO: 29179-20-2
• Molecular Formula: C14H14O
• Molecular Weight: 198.265
• Mol File: 29179-20-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-Cyclohexen-1-one, 3-(2-phenylethenyl)-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Cyclohexen-1-one, 3-(2-phenylethenyl)-, (E)-(29179-20-2)
• EPA Substance Registry System: 2-Cyclohexen-1-one, 3-(2-phenylethenyl)-, (E)-(29179-20-2)

Safety Data

• Hazardous Substances Data: 29179-20-2(Hazardous Substances Data)

Upstream product

• 1193-18-6 3-methylcyclohexen-2-one 
• 100-52-7 benzaldehyde 
• 5682-75-7 3-chloro-2-cyclohexenone 
• 536-74-3 phenylacetylene 
• 588-72-7 [(E)-2-bromoethenyl]benzene 
• 5323-87-5 3-Ethoxycyclohex-2-en-1-one 
• 101773-31-3 3-<(trimethylsilyl)methyl>cyclohexanone enol silyl ether 
• 930-68-7 cyclohexenone 
• 504-02-9 1,3-cylohexanedione 
• 100-42-5 styrene 
• 77708-66-8 3-oxocyclohex-1-en-1-yl 4-methylbenzenesulfonate 
• 108162-13-6 Z-styryl n-butyltelluride 
• 88841-83-2 3-(Phenylseleno)-2-cyclohexen-1-one 
• 1119-40-0 Dimethyl glutarate 

Downstream Products

• 1402434-84-7 (S,E)-3-ethyl-3-styrylcyclohexanone 

Relevant articles and documents

First examples of a tosylate in the palladium-catalyzed Heck cross coupling reaction

The palladium-catalyzed cross coupling Heck reaction of tosylate (2) and methyl acrylate has been developed as an efficient method for carbon-carbon bond formation. The tosylate (2) was reacted with methyl acrylate using palladium acetate as catalyst to p

Carbonyl transposition on organoselenium compounds

Carbonyl conjugated vinylic selenides undergo 1,3 and 1,5-carbonyl transposition sequences through organometallic reagents addition reactions followed by acid hydrolysis.

Stereoselective Synthesis of Conjugated Dienones via the Palladium-Catalyzed Cross-Coupling Reaction of 1-Alkenylboronates with 3-Halo-2-alken-1-ones

The synthesis of conjugated dienones by means of palladium-catalyzed cross-coupling reaction between (E)-1-alkenyl-1,3,2-benzodioxaboroles or diisopropyl (Z)-1-hexenylboronate with 3-halo-2-alken-1-ones is described.