Benzyl Cinnamate
Structural Formula Vector Image
Title: Benzyl Cinnamate
CAS Registry Number: 103-41-3
CAS Name: 3-Phenyl-2-propenoic acid phenylmethyl ester
Additional Names: trans-cinnamic acid benzyl ester; cinnamein
Molecular Formula: C16H14O2
Molecular Weight: 238.28
Percent Composition: C 80.65%, H 5.92%, O 13.43%
Line Formula: C6H5CH=CHCOOCH2C6H5
Literature References: Constituent of storax, Peru and Tolu balsams: Tschirch, Trog, Arch. Pharm. 232, 70 (1894); Tschirch, Oberländer, ibid. 559. Prepn: Volwiler, Vliet, J. Am. Chem. Soc. 43, 1672 (1921); Eliel, Anderson, ibid. 74, 547 (1952); Bender, Zerner, ibid. 84, 2550 (1962). Toxicity study: P. M. Jenner et al., Food Cosmet. Toxicol. 2, 327 (1964).
Properties: Crystals from 95% ethanol; sweet odor of balsam. mp 39°; also reported as mp 33-34° (Volwiler, Vliet). Dec on distillation at ordinary pressure; bp0.5 154-157°, bp5 195-200°, bp22 228-230°. Practically insol in water, propylene glycol and glycerin. Sol in alc, ether, oils. LD50 orally in rats: 5530 mg/kg (Jenner).
Melting point: mp 39°; mp 33-34° (Volwiler, Vliet)
Boiling point: bp0.5 154-157°; bp5 195-200°; bp22 228-230°
Toxicity data: LD50 orally in rats: 5530 mg/kg (Jenner)
Use: In artificial flavors, in perfumes, mainly as a fixative.

Other Monographs:
Berberis AristataViolaceinCelery SeedBeryllium Sodium Fluoride
GougerotinTopotecanTerfenadineFlupirtine
ChlorbensideSodium Ferric GluconateCoumafurylKetipic Acid
Interleukin-2IohexolRed Fluorescent ProteinNizatidine
©2006-2023 DrugFuture->Chemical Index Database