1448857-21-3

Basic information

• Product Name: (E)-1-(4-methoxyphenyl)-3-phenylpent-2-en-1-one
• Synonyms: (E)-1-(4-methoxyphenyl)-3-phenylpent-2-en-1-one
• CAS NO: 1448857-21-3
• Molecular Weight: 266.34
• Mol File: 1448857-21-3.mol

Chemical Properties

• CAS DataBase Reference: (E)-1-(4-methoxyphenyl)-3-phenylpent-2-en-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-(4-methoxyphenyl)-3-phenylpent-2-en-1-one(1448857-21-3)
• EPA Substance Registry System: (E)-1-(4-methoxyphenyl)-3-phenylpent-2-en-1-one(1448857-21-3)

Safety Data

• Hazardous Substances Data: 1448857-21-3(Hazardous Substances Data)

Upstream product

• 98-80-6 phenylboronic acid 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 55314-57-3 ethyl pent-2-ynoate 
• 29743-74-6 ethyl (E)-3-phenyl-2-pentenoate 

Downstream Products

• 1448857-48-4 1-(4-methoxyphenyl)-3-methyl-3-phenylpentan-1-one 
• 1448857-47-3 1-(4-methoxyphenyl)-3-methyl-3-phenylpentan-1-one 
• 4887-10-9 (R)-3-methyl-3-phenylpentanoic acid 

Relevant articles and documents

Effect of multinuclear copper/aluminum complexes in highly asymmetric conjugate addition of trimethylaluminum to acyclic enones

Al and friends: Asymmetric conjugate addition of Me3Al to β,β-disubstituted α,β-unsaturated ketones in the presence copper and L1 leads to a highly efficient construction of an all-carbon-substituted chiral quaternary center. This result is the first example of an asymmetric conjugate addition of Me3Al to acyclic enones to give a chiral quaternary carbon center with excellent yield and enantioselectivity under mild reaction conditions. Copyright