944130-58-9

Basic information

• Product Name: 2-benzylprop-2-en-1-yl acetate
• Synonyms: 2-benzylprop-2-en-1-yl acetate
• CAS NO: 944130-58-9
• Molecular Weight: 190.242
• Mol File: 944130-58-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-benzylprop-2-en-1-yl acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzylprop-2-en-1-yl acetate(944130-58-9)
• EPA Substance Registry System: 2-benzylprop-2-en-1-yl acetate(944130-58-9)

Safety Data

• Hazardous Substances Data: 944130-58-9(Hazardous Substances Data)

Upstream product

• 30457-89-7 2-benzylallyl alcohol 
• 108-24-7 acetic anhydride 
• 820-71-3 methallyl acetate 
• 98-80-6 phenylboronic acid 
• 3240-34-4 [bis(acetoxy)iodo]benzene 
• 90252-79-2 3-benzylbut-3-enoic acid 

Downstream Products

• 944130-45-4 (S,E)-2-[3-(2-benzylallyloxy)pent-1-enyl]furan 

Relevant articles and documents

Hypervalent iodine(III)-Mediated oxidative decarboxylation of β,γ-unsaturated carboxylic acids

A novel oxidative decarboxylation of β,γ-unsaturated carboxylic acids mediated by hypervalent iodine(III) reagents is described. The decarboxylative C-O bond forming reaction proceeded in the presence of PhI(OAc)2 to give the corresponding allylic acetates. In addition, decarboxylative C-N bond formation was achieved by utilizing hypervalent iodine(III) reagents containing an I-N bond. Mechanistic studies suggest the unique reactivity of hypervalent iodine reagents in this ionic oxidative decarboxylation.

Organoleptic Compounds and Their Use in Perfume Compositions

The present invention is directed to the novel cyclohexyl, cyclopentyl and acyclic ester compounds of the general formula: wherein R and R1 independently represent a hydrogen or a straight, branched or cyclic hydrocarbon consisting of less than