| Identification | Back Directory | [Name]
Cinnamylcetate | [CAS]
21040-45-9 | [Synonyms]
Cinnamylcetate
(E)-cinnamyl acetate
(E)-Cinnamyl alcohol acetate
Acetic acid (E)-cinnamyl ester
(E)-3-Phenyl-2-propenyl=acetate
(2E)-3-Phenyl-2-propen-1-ylacetate
Acetic acid (E)-3-phenylallyl ester
(E)-3-Phenyl-2-propene-1-ol acetate
2-Propen-1-ol, 3-phenyl-, acetate, (2E)-
2-Propen-1-ol,3-phenyl-, 1-acetate, (2E)-
Acetic acid (2E)-3-phenyl-2-propenyl ester
Cinnamyl acetate/trans-Cinnamyl acetate/(E)-Cinnamyl acetate | [Molecular Formula]
C11H12O2 | [MDL Number]
MFCD00008722 | [MOL File]
21040-45-9.mol | [Molecular Weight]
176.21 |
| Chemical Properties | Back Directory | [Boiling point ]
265°C (estimate) | [density ]
1.0567 | [refractive index ]
1.5425 (estimate) | [solubility ]
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | [form ]
Oil | [Odor]
at 100.00 %. sweet floral spicy balsam | [Odor Type]
spicy | [LogP]
2.620 |
| Hazard Information | Back Directory | [Chemical Properties]
Cinnamyl Acetate is the only ester
of cinnamic alcohol of any importance. trans-Cinnamyl acetate occurs in cassia
oil and is a colorless liquid with a sweet-floral-fruity, slightly balsamic odor. It is a
good fixative and is used in blossom compositions (e.g., lilac and jasmine) and for
oriental notes. In flavor compositions, it is used for cinnamon-fruity effects. | [Uses]
(E)-Cinnamyl acetate, isolated from cinnamon fruit stalks, has antioxidant activities[1][2]. | [Definition]
ChEBI: Cinnamyl acetate is an acetate ester resulting from the formal condensation of cinnamyl alcohol with acetic acid. Found in cinnamon leaf oil. It has a role as a fragrance, a metabolite and an insecticide. It is functionally related to a cinnamyl alcohol. | [References]
[1] Thomas, A. F., et al. Two New Sesquiterpenoid Ketones from Cassia Oil. Helvetica Chimica Acta, 63(6)
[2] Guddadarangavvanahally K Jayaprakasha, et al. Volatile Constituents from Cinnamomum zeylanicum Fruit Stalks and Their Antioxidant Activities. J Agric Food Chem. 2003 Jul 16;51(15):4344-8. DOI:10.1021/jf034169i |
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