1246566-87-9

Basic information

• Product Name: (E)-2,2,2-trifluoro-N-phenethyl-N-(1-phenylhex-4-en-3-yl)acetamide
• Synonyms: (E)-2,2,2-trifluoro-N-phenethyl-N-(1-phenylhex-4-en-3-yl)acetamide
• CAS NO: 1246566-87-9
• Molecular Weight: 375.434
• Mol File: 1246566-87-9.mol

Chemical Properties

• CAS DataBase Reference: (E)-2,2,2-trifluoro-N-phenethyl-N-(1-phenylhex-4-en-3-yl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-2,2,2-trifluoro-N-phenethyl-N-(1-phenylhex-4-en-3-yl)acetamide(1246566-87-9)
• EPA Substance Registry System: (E)-2,2,2-trifluoro-N-phenethyl-N-(1-phenylhex-4-en-3-yl)acetamide(1246566-87-9)

Safety Data

• Hazardous Substances Data: 1246566-87-9(Hazardous Substances Data)

Upstream product

• 56539-56-1 (E)-6-phenyl-2-hydroxy-hex-3-ene 
• 33046-41-2 (E)-6-phenyl-3-hexen-2-one 

Relevant articles and documents

Catalyst versus substrate induced selectivity: Kinetic resolution by palladacycle catalyzed allylic imidate rearrangements

Making chairs: A kinetic resolution of allylic imidates by planar chiral palladacycles is described which is the result of high face selectivity for olefin coordination to the catalyst and inherent substrate selectivity. These studies confirm that planar chiral palladacycles mainly operate via (half)chair-like transition states/intermediates.