Phenyl-propyl esters

Cinnamic acid, 3-phenyl propyl ester. See 3-Phenylpropyl cinnamate Cinnamic alcohol. SeeCinnamyl alcohol, Cinnamic aldehyde. See Cinnamal Cinnamic aldehyde ethylene glycol acetal. See Cinnamaldehyde ethylene glycol acetal Cinnamic chloride. See Cinnamoyl chloride Cinnamol. See Styrene Cinnamomum camphora. See Camphor Cinnamomum camphora oil. See Camphor (Cinnamomum camphora) oii Cinnamomum cassia. See Cinnamon (Cinnamomum cassia) extract Cinnamon (Cinnamomum cassia) Cinnamon (Cinnamomum cassia) oii... [Pg.953]

Isobutyric acid 2-phenoxyethyl ester. See Phenoxyethyl isobutyrate Isobutyric acid 3-phenyl propyl ester. See 3-Phenylpropyl isobutyrate Isobutyric acid, p-tolyl ester. See p-Tolyl isobutyrate... [Pg.2214]

Synonyms Cinnamic acid, 3-phenyl propyl ester Hydrocinnamyi cinnamate 3-Phenyl-2-propenoic acid 3-phenyl propyl ester Phenyipropyl cinnamate 3-Phenyl propyl 3-phenyl-2-propenoate... [Pg.3334]

Propenoic acid, 3-phenyl-, 3-phenyl propyl ester... [Pg.3334]

C2SH32O4 heptanedioic acid bis-(2-phenyl-propyl) ester 97117-21-0... [Pg.922]

C11H14 02 acetic acid 3-phenyl-propyl ester 122-72-5... [Pg.350]

Phenyl-propyl alcohol, CgH. CHj. CH.2. CHj. OH, is the next highest homologue of phenyl-ethyl alcohol, and is also known as hydro-cinnamyl alcohol. Like the last described bodies it has been known for many years, its first preparation being described in the Aivnalen (188, 202). It occurs as a cinnamic acid ester in storax, and as an acetic ester in cassia oil. It is prepared synthetically by the reduction of cinnamyl alcohol with sodium amalgam and water, or by the reduction of cinnamic or benzyl acetic esters with sodium and absolute alcohol. It has the following characters —... [Pg.128]

Phenyl-propyl CinTiamate.—This ester occurs in storax, and has a perfume res mbling that balsamic substance. It has the formula... [Pg.175]

To a solution of 4 g of sodium in 200 ml of n-propanol is added 39 g of homovanillic acid-n-propyl ester (boiling point 160°C to 162°C/4 mm Hg) and the mixture is concentrated by evaporation under vacuum. After dissolving the residue in 200 ml of dimethylformamide and the addition of 0.5 gof sodium iodide, 26.2 g of chloracetic acid-N,N-diethylamide are added drop-wise with stirring at an internal temperature of 130°C, and the mixture is further heated at 130°C for three hours. From the cooled reaction mixture the precipitated salts are removed by filtering off with suction. After driving off the dimethylformamide under vacuum, the product is fractionated under vacuum, and 44.3 g of 3-methoxy-4-N,N-diethylcarbamido-methoxy phenyl acetic acid-n-propyl ester are obtained as a yellowish oil of boiling point 210°C to 212°C/0,7 mm Hg,... [Pg.1310]

C2yH27N709S2 78968-24-8) see Temocillin [23 -(2ot,5ot,6a)]-6-[[l,3-dioxo-3-(phenylmethoxy)-2-(3-thienyl)propyl]amino]-6-methoxy-33-dimethyl-7-oxo-4-thid-l-azabicyc)o[3.2.0]beptane-2-carboxyIic acid phenyl-methyl ester... [Pg.2368]

Methyl ester (Me-est Methyl 2-(3-Cyano-4-(2-metylpropoxy)-phenyl)- 4-methyl-thiazole-5-carboxylate) and propyl ester (Pr-est Propyl 2-(3-Cyano-4-(2-methyl-propoxy)-phenyl)-4-methyl-thiazole-5-carboxylate) were synthesized (Fig. 11.1)... [Pg.125]

N1 - ISONIPECOTIC ACID, 1-METHYL-6-PHENYL-, ETHYL ESTER and 10-<3-<DIMETHYLAMINO>PROPYL) PHENOTHIAZXNE (2a)... [Pg.127]

H5C,-P[0-CH2-CH(CH3)2]2 C1-CH2-COOC2H= 140-160 0,5 (Ethoxy carbonyl-methyl)-phenyl-phosphinsdure- (2-methyl-propyl-ester) 76 163-167 3 (0,4) 533... [Pg.207]

Thiophosphonigsaure-ester-halogenide unterliegen der Michaelis Arbuzov-Reaktion mit Alkylhalogeniden866, z.B. kann so Phenyl-propyl-thiophosphinsaure-chlorid in 62%iger Ausbeute gewonnen werden ... [Pg.248]

Acetoxy-ethyl)phenyl- -ethylester XII/1, 258 (2-Acetoxy-propyl)-methyl- -(2-methyl-propyl-ester) E2, 189... [Pg.1017]

Phenyl-propyl- -chlorid E2, 248 2-Propinyl- -ester E2, 222 1-Propinyl- -S-ester E2, 222 -S-(2-vinylthio-ethylester) E2, 226... [Pg.1092]

Similarly, attempts to generate the azaallyl complex 401 from N-TMS phenyl propyl amine result in formation of the aromatic metallation product 43 after only 45 min at 65 °C (Scheme 14). Interception of the intermediate 21 with (rac)-DPEC gives the homophenylalanine ester 381 in 96% de and 53% yield [24]. [Pg.36]

Thiocarbamidsaure N,N-Dimethyl- -0-(3-methoxy-phenylester) E4, 435 (Cl -> NR2) N-Hydroxy-N-phenyl- -S-propyl-ester E4, 331 (Cl - N(OH)-Ar] Thiophen... [Pg.765]

SYNS HETEROFOS PHOSPHOROTHIOIC ACID, o-ETHYL o-PHENYL S-PROPYL ESTER PHOSTIL... [Pg.710]

S-PROPYL ESTER 0-ETHYL-0-(4-(METHYL-THIO)PHENYL) S-PROPYL PHOSPHORODTTHIOATE HELOTHION... [Pg.1296]

ISOCYANIC ACID, OCTADECYL ESTER see OBGOOO ISOCYANIC ACID, PHENYL ESTER see PFK250 ISOCYANIC ACID, PROPYL ESTER see PNPOOO ISOCYVsTC ACID, o-TOLYL ESTER see IKG725 ISOCYANIC ACID, 3-(TRIETHOXYSILYL)PROPYL ESTER see IKG900 ISOCYANIC ACID, (m-... [Pg.1735]

PHOSPHOROTHIOIC ACID, 0-(4-(AMINOSULFONYL)PHENYL) 0,0-DIMETHYL ESTER (9CI) see CQL250 PHOSPHOROTHIOIC ACID-S-(((l-CYANO-l-METHYL-ETHYL)CARBAMOYL)METHYL)-0,0-DIETHYL ESTER see PHK250 PHOSPHOROTHIOIC ACID, o-(2,4-DICHLOROPHENYL) o-ETHYL S-PROPYL ESTER see EEE200... [Pg.1841]

PHOSPHOROTHIOIC ACID, o-ETHYL o-PHENYL S-PROPYL ESTER see HBU415 PHOSPHOROTHIOIC ACID TRIETHYLENETRIAMIDE see TFQ750 PHOSPHOROTHIOIC TRICHLORIDE see TFOOOO PHOSPHOROTHIONIC TRICHLORIDE see TFOOOO PHOSPHOROTRITHIOUS ACID, S,S,S-TRIBUTYL ESTER see TIG250... [Pg.1841]

The optically active arsinous acid esters 128-134 and the arsinthious acid ester 135 have been used to prepare optically active tertiary arsines (Table 7). When the arsine sulphide 136 was heated in benzene with n-butyl or -propyl bromide, ethyl bromide was eliminated and there was a reversal in the sign of the rotation, which was attributed to the formation of the inverted n-butyl and n-propyl esters of (p-carboxyphenyl)phenyl-arsinthious acid, 137a and 137b, respectively (equation 18) . [Pg.133]

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