Phenethyl cinnamate

Propenoic acid, 3-phenyl-, phenylethyl ester phenethyl cinnamate ... [Pg.1168]

Cinnamic acid phenethyl ester. See Phenethyl cinnamate... [Pg.953]

Phenethyl carbinol. See Hydrocinnamic alcohol Phenethyl cinnamate CAS 103-53-7 El NECS/ELINCS 203-120-3 FEMA 2863... [Pg.3284]

P-Phenethyl cinnamate. See Phenethyl cinnamate Phenethyl crotonate... [Pg.3284]

D isomer. See Carbetamide Phenylethyl carbinol. See Hydrocinnamic alcohol 1-Phenyl-1-propanol Phenylethyl cinnamate 2-Phenylethyl cinnamate. See Phenethyl cinnamate Phenyl ethyl cyclohexyl ether. See Cyclohexyl phenethyl ether... [Pg.3318]

Phenethyl benzoate Phenethyl butyrate Phenethyl cinnamate Phenethyl formate Phenethyl isobutyrate Phenethyl isovalerate Phenethyl 2-methylbutyrate Phenethyl phenylacetate Phenethyl propionate Phenethyl salicylate Phenethyl senecioate Phenethyl tiglate Phenoxyacetic acid Phenoxyethyl isobutyrate Phenylacetaldehyde Phenylacetaldehyde 2,3-butylene glycol acetal Phenylacetaldehyde diisobutyl acetal Phenylacetaldehyde dimethyl acetal Phenylacetaldehyde glyceryl cyclic acetals Phenyl acetate... [Pg.5286]

Phenethyl benzoate Phenethyl butyrate Phenethyl cinnamate Phenethyl formate Phenethyl hexanoate... [Pg.5290]

Perillyl alcohol Petitgrain oil a-Phellandrene (+)-a-Phellandrene Phenethyl anthranilate Phenethyl benzoate Phenethyl butyrate Phenethyl cinnamate Phenethyl crotonate Phenethyl 2-ethyl butyrate Phenethyl formate Phenethyl isobutyrate Phenethyl isothiocyanate Phenethyl isovalerate Phenethyl methacrylate Phenethyl 2-methyl butyrate Phenethyl methyl ethyl carbinyl acetate Phenethyl phenylacetate Phenethyl pivalate Phenethyl propionate... [Pg.5324]

Cinnamyl phenylacetate Phenethyl cinnamate C17H16O3 Eugenyl benzoate (Ci7Hi60s)n... [Pg.7096]

Phenethyl alcohol is qualitatively and quantitatively one of the most important fragrance substances that belongs to the class of araliphatic alcohols. Its lower homologue (benzyl alcohol) and higher homologue (dihydrocinnamic alcohol) also have characteristic odor properties, but are more frequently used in the form of their esters. Cinnamic alcohol, the most important unsaturated araliphatic alcohol, is valuable for both fragrances and flavors. [Pg.97]

Honey Allyl phenoxyacetate, phenylaceiate Benzyl cinnamate Carvacryl acetate Cinnamyl butyrate p-Cresyl acetate p-Cresyl ethyl ether /rt-Cresyl phenylaceiate />-Cresyl phenylaceiate Cyclohexyl phenylacctate Ethyl phenoxyacetate. phenylaceiate Guaiol phenylaceiate Isobutyl phenylaceiate Linalyl butyrate Methyl phenylaceiate Phenethyl acetate, butyrate, phenylaceiate Phenylacetic acid Propyl phenylaceiate Santalyl phenylaceiate. [Pg.648]

Some of the widely used synthetic fixatives are amyl benzoate, phenethyl, phenyl acetate, cinnamic alcohol esters, acetophenone, musk ambrette, musk ketone, musk xylols, vanillin, coumarin, etc. [41]. [Pg.153]

Diphenyl-sulfon-3,3 -disulfohydrazide C12H14O2 Benzyl tiglate Cinnamyl propionate Isopropyl cinnamate 1 -(p-Methoxyphenyl)-l -penten-3-one Phenethyl methacrylate Prenyl benzoate C12H14O3 Acetisoeugenol Ethyl methoxycinnamate Ethyl methyl phenylglycidate Eugenyl acetate 2-Phenoxyethyl methacrylate C12H14O4... [Pg.7077]

The Bischler-Napieralski reaction [20] and the Pictet-Gams reaction [22] are both known as typical methods for the construction of the isoquinoline framework as described in Sect 2. Gambon et al. synthesized l-(trifluoromethyl)isoquinolines via the Bischler-Napieralski reaction of A(-(phenethyl)trifluoroacetamides, [104] whereas Simig et al. utilized the Pictet-Gams reaction of Af-(2-aryl-3,3,3-trifluoro-2-methoxypropyl)amides of acetic or cinnamic acids for the synthesis of 4-(trifluo-romethyl)isoquinolines (Scheme 30) [105]. [Pg.197]

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