1542075-20-6

Basic information

• Product Name: (+)-(1R)-1-phenylprop-2-en-1-yl (2E,4E)-hexa-2,4-dienoate
• Synonyms: (+)-(1R)-1-phenylprop-2-en-1-yl (2E,4E)-hexa-2,4-dienoate
• CAS NO: 1542075-20-6
• Molecular Weight: 228.291
• Mol File: 1542075-20-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (+)-(1R)-1-phenylprop-2-en-1-yl (2E,4E)-hexa-2,4-dienoate(CAS DataBase Reference)
• NIST Chemistry Reference: (+)-(1R)-1-phenylprop-2-en-1-yl (2E,4E)-hexa-2,4-dienoate(1542075-20-6)
• EPA Substance Registry System: (+)-(1R)-1-phenylprop-2-en-1-yl (2E,4E)-hexa-2,4-dienoate(1542075-20-6)

Safety Data

• Hazardous Substances Data: 1542075-20-6(Hazardous Substances Data)

Upstream product

• 1240492-42-5 bis(2-ethylhexyl) (2E)-3-phenylprop-2-en-1-yl phosphate 
• 24634-61-5 potassium sorbate 
• 3658-48-8 bis(2-ethylhexyl)phosphite 
• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 

Relevant articles and documents

Enantio- and regioselective iridium-catalyzed allylic esterification

A highly enantioselective and regioselective Ir-catalyzed allylic esterification is described, in which branched allylic esters are synthesized directly. Carboxylates were used as nucleophiles and linear allylic phosphates as electrophiles. In some cases the allylic substitution reaction was found to be accompanied by a kinetic resolution process, which causes a change of the enantiomeric excess.