67590-77-6

Basic information

• Product Name: 2-Hexenylbenzene.
• Synonyms: 2-Hexenylbenzene.
• CAS NO: 67590-77-6
• Molecular Formula: C₁₂H₁₆
• Molecular Weight: 160.25544
• Mol File: 67590-77-6.mol
• Article Data: 23

Chemical Properties

• Melting Point: -30.6°C (estimate)
• Boiling Point: 221.18°C (estimate)
• Appearance: /
• Density: 0.8898
• Refractive Index: 1.5058
• CAS DataBase Reference: 2-Hexenylbenzene.(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Hexenylbenzene.(67590-77-6)
• EPA Substance Registry System: 2-Hexenylbenzene.(67590-77-6)

Safety Data

• Hazardous Substances Data: 67590-77-6(Hazardous Substances Data)

Upstream product

• 13633-27-7 1-(hexa-1,2-dienyl)benzene 
• 182740-29-0 (Z)-Dodec-3-en-1,5-diin 
• 140-88-5 ethyl acrylate 
• 192872-21-2 3-propylallyl methyl carbonate 
• 100-58-3 phenylmagnesium bromide 
• 17869-38-4 3-trimethylsiloxy-1-hexene 
• 72106-89-9 trans-1-(trimethylsiloxy)hex-2-ene 
• 120989-99-3 [(2E)-hex-2-en-1-yloxy]benzene 
• 2497-18-9 2-hexenyl acetate 
• 143-66-8 sodium tetraphenyl borate 
• 627-19-0 1-Pentyne 
• 300-57-2 allylbenzene 
• 7642-15-1 (Z)-oct-4-ene 
• 123-72-8 butyraldehyde 

Downstream Products

• 1370038-00-8 butyl (E)-3-(2-((Z)-hex-2-enyl)phenyl)acrylate 
• 1370037-99-2 butyl (E)-3-(2-((E)-hex-2-enyl)phenyl)acrylate 

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

Method for synthesizing 1,2-dissubstituted olefin compounds by alkyne alkylation

The invention discloses a method for synthesizing 1,2-dissubstituted olefin compounds by high-selectivity alkyne alkylation. The method comprises the following specific steps: a photosensitizer, an alkyne compound represented as the formula I and hantzsch