78633-32-6

Basic information

• Product Name: Benzene, 2-hexenyl-, (Z)-
• Synonyms: (E)-1-phenyl-2-hexene;(E)-1-Phenylhex-2-ene
• CAS NO: 78633-32-6
• Molecular Formula: C12H16
• Molecular Weight: 160.259
• Mol File: 78633-32-6.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: Benzene, 2-hexenyl-, (Z)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 2-hexenyl-, (Z)-(78633-32-6)
• EPA Substance Registry System: Benzene, 2-hexenyl-, (Z)-(78633-32-6)

Safety Data

• Hazardous Substances Data: 78633-32-6(Hazardous Substances Data)

Upstream product

• 110-62-3 pentanal 
• 300-57-2 allylbenzene 
• 7642-15-1 (Z)-oct-4-ene 
• 2497-18-9 2-hexenyl acetate 
• 143-66-8 sodium tetraphenyl borate 
• 14850-23-8 trans-4-Octene 
• 627-19-0 1-Pentyne 
• 123-72-8 butyraldehyde 
• 536-74-3 phenylacetylene 
• 591-50-4 iodobenzene 
• 2497-18-9 (E)-2-hexen-1-yl acetate 
• 4798-44-1 1-hexene-3-ol 
• 928-95-0 (E)-2-Hexen-1-ol 
• 120989-99-3 [(2E)-hex-2-en-1-yloxy]benzene 

Relevant articles and documents

Aziridine Opening via a Phenonium Ion Enables Synthesis of Complex Phenethylamine Derivatives

We report that the treatment of unsymmetrical 2,3-disubstituted aziridines with TiCl4 yields β-phenethylamine products via the intermediacy of a phenonium ion. Derivatization of the products obtained via this method is demonstrated. Computational analysis of the reaction pathway provides insight into the reaction mechanism, including the selectivity of the phenonium opening.

P/N Heteroleptic Cu(I)-Photosensitizer-Catalyzed Deoxygenative Radical Alkylation of Aromatic Alkynes with Alkyl Aldehydes Using Dipropylamine as a Traceless Linker Agent

A deoxygenative radical alkylation of aromatic alkynes with alkyl aldehydes for the preparation of allylarenes has been successfully achieved. This transformation is accomplished through the reaction of alkyl aldehydes with alkynes in the presence of dipr

OLEFIN METATHESIS CATALYSTS

This invention relates generally to metathesis catalysts and the use of such catalysts in the metathesis of olefins and olefin compounds, more particularly, in the use of such catalysts in Z and E selective olefin metathesis reactions. The invention has utility in the fields of organometallics and organic synthesis.