cinnamate


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Related to cinnamate: Methyl cinnamate

cinnamate

[′sin·ə‚māt]
(organic chemistry)
A salt of cinnamic acid, containing the functional group C9H7O2‒.
McGraw-Hill Dictionary of Scientific & Technical Terms, 6E, Copyright © 2003 by The McGraw-Hill Companies, Inc.
References in periodicals archive ?
In 1928, in the USA, one of the first sunscreens had benzyl cinnamate in its composition, but its use was limited.
Holzgrabe, "Anti-schistosomal activity of cinnamic acid esters: Eugenyl and thymyl cinnamate induce cytoplasmic vacuoles and death in schistosomula of Schistosoma mansoni," Molecules, vol.
(c) Including possibly 1-(3-propoxyprop-1-enyl)benzene, cinnamyl formate, cinnamic acid, benzyl cinnamate, 4,4-diphenylcyclohexane-1,5-dienyl acetate, and other condensation products that could be identified by GC-MS because of their large molecular weights.
Peak number Compound RRT(min) % 1 Benzaldehyde 6.714 4.59 2 Phenol 7.357 0.13 3 Phenylacetaldehyde 9.345 0.40 4 Phenyl methyl ketone 10.095 0.17 5 Benzyl formate 10.486 0.40 6 Benzoic acid 13.917 0.99 7 Cinnamaldehyde 15.410 0.31 8 Phenylacetic acid 16.741 0.31 9 Trans-Cinnamaldehyde 17.349 74.70 10 Cinnamic acid 22.955 15.47 11 Cinnamic acid trimethylsilyl ester 25.870 0.17 12 l,4-Diphenyl-l,3-butadiene 35.332 0.13 13 trans,trans-l,4-Diphenyl-l,3-butadiene 38.291 0.21 14 Benzyl cinnamate 40.090 0.47 15 1,2-Dibenzoylethane 42.150 0.38 16 3-cyclopenten-1-one 42.385 0.51 17 Acetyl tributyl citrate 43.613 0.34 18 2-Methylphenanthro[3,4-d][l,3] 44.153 0.10 oxazol-10-ol RRT = relative retention time.
Ethyl hexanoate and (E)-ethyl cinnamate compounds present in wine samples are described as fruity, strawberry, sweet, and floral flavor compounds (AZNAR et al., 2001).
Another is (http://www.chemspider.com/Chemical-Structure.21105944.html) methyl cinnamate with a spicy note.
Phenylalanine ammonia-lyase and hydroxy cinnamate: CoA ligase in maize mesocotyls inoculated with Helminthosporium maydis or Helminthosporium carbonum.
E-Methyl Cinnamate. [sup.1]H NMR (400 MHz, CD[Cl.sub.3]): [delta] 7.63 (d, 7 = 16.0 Hz, 1H), 7.45 (dd, 7 = 6.6, 3.0 Hz, 2H), 7.31 (dd, 7 = 6.5, 3.7 Hz, 2H), 7.18 (s, 1H), 6.37 (d, 7 = 16.0 Hz, 1H), 3.74 (s, 3H).
[17] on cinnamate supplementation in high cholesterol-fed rats showed that cinnamate, a phenolic compound found in cinnamon bark, lowers cholesterol levels by inhibiting the HMG-CoA reductase activity.
Concentrations of ethyl cinnamate, a cinnamon flavor, differed significantly (P < 0.001) compared to the Control samples.