69371-59-1

Basic information

• Product Name: 5-Hexen-2-one, 6-phenyl-
• CAS NO: 69371-59-1
• Molecular Formula: C12H14O
• Molecular Weight: 174.243
• Mol File: 69371-59-1.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 5-Hexen-2-one, 6-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Hexen-2-one, 6-phenyl-(69371-59-1)
• EPA Substance Registry System: 5-Hexen-2-one, 6-phenyl-(69371-59-1)

Safety Data

• Hazardous Substances Data: 69371-59-1(Hazardous Substances Data)

Upstream product

• 4393-06-0 1-Phenyl-2-propen-1-ol 
• 141-97-9 ethyl acetoacetate 
• 108400-97-1 ethyl (4E)-2-acetyl-5-phenylpent-4-enoate 
• 100-52-7 benzaldehyde 
• 1493-13-6 trifluorormethanesulfonic acid 
• 105-45-3 acetoacetic acid methyl ester 
• 4392-24-9 3-bromo-1-phenyl-1-propenyl bromide 
• 673-32-5 1-Phenylprop-1-yne 
• 67-64-1 acetone 
• 109-49-9 5-Hexen-2-one 
• 98-80-6 phenylboronic acid 
• 5720-07-0 4-methoxyphenylboronic acid 
• 369-57-3 benzenediazonium tetrafluoroborate 
• 104-54-1 3-Phenylpropenol 

Downstream Products

• 134025-31-3 N-Methoxy-1-phenyl-1-hexen-5-one oxime 
• 134038-98-5 N-Methyl-1-methyl-5-phenylpent-4-enylamine 
• 14171-89-2 1-phenyl-5-hexanone 
• 134038-99-6 2-Benzoyl-1-methoxy-5-methylpyrrolidine 
• 134025-26-6 N-Methoxy-1-methyl-5-phenylpent-4-enylamine 
• 134025-21-1 cis-2-Benzyl-1,5-dimethylpyrrolidine 
• 182194-89-4 Toluene-4-sulfonic acid (E)-1-methyl-5-phenyl-pent-4-enyl ester 
• 38488-04-9 (2R*,6R*)-2-methyl-6-phenyltetrahydro-2H-pyran 
• 127047-14-7 5-hydroxy-1-phenyl-hexene-⁽¹⁾ 

Relevant articles and documents

Synthesis of Cyclic β-Silylalkenyl Triflates via an Alkenyl Cation Intermediate

Trimethylsilylalkyne derivatives are transformed into cyclic β-silylalkenyl triflates through cationic cyclization and subsequent trapping of the alkenyl cation by a triflate anion. β-Silylcyclohexenyl triflates and 3-trimethylsilyl-1,4-dihydronaphth-2-yl

Cooperative Palladium/Proline-Catalyzed Direct α-Allylic Alkylation of Ketones with Alkynes

The cooperative palladium/l-proline-catalyzed direct α-allylic alkylation of ketones with alkynes is achieved. This reaction exhibits high atom economy since a leaving group is not liberated and a stoichiometric amount of extra oxidant is not needed. A br

Pd(0)-catalyzed 1,1-diarylation of ethylene and allylic carbonates

An efficient protocol for the one-step synthesis of biologically relevant 1,1-diarylalkanes has been described. This reaction introduces two different aryl groups across the terminal end of simple feedstock alkenes such as ethylene and allylic carbonates.