Styryl carbinol

SYNS CINNAMIC ALCOHOL CINNAMYL ALCOHOL, SYNTHETIC FEMA No. 2294 y-PHENYLALLYL ALCOHOL 3-PHENYLALLYL ALCOHOL 3-PHENYL-2-PROPEN-1-OL STYRONE STYRYL CARBINOL... [Pg.371]

Beilstein Handbook Reference) AI3-00949 Alkohol skoricovy BRN 1903999 CCRIS 3191 Cinnamic alcohol Cinnamyl alcohol EINECS 203-212-3 FEMA No. 2294 3-Fenyl-2-propen-1-ol HSDB 5011 NSC 8775 Peruvin 3-Phenylallyl alcohol o-Phenylallyl alcohol Phenyl-2-propen-1-ol 1-Phenylprop-1-en-3-ol 3-Phenyl-2-propen-1-ol 3-Phenyl-2-propenol 2-Propen-1-ol, 3-phenyl- 2-Propen-yl-ol, 3-phenyl- Propenoic xid, 3-phenyl-, (trans)- Styrone Styryl alcohol Styryl carbinol Zimtalcohol. Used in perfumery and in deodorants. Crystals mp = 33-35° bp 249-250° dJJ = 1.0397 soluble in H2O, organic solvents. [Pg.148]

Maurin, M.B., Addicks, WJ., Rowe, S.M. and Hogan, R. (1993) Physical chemical properties of alpha styryl carbinol antifungal agents. Pharm. Res. 10 309-312. [Pg.324]

Maurin MB, Addicks W], Rowe SM and Hogan R, Physicochemical properties of a-styryl carbinol antifungal agents, Pharm. Res., 10, 30 312 (1993)."... [Pg.176]

Synonyms Cinnamic alcohol 3-Phenylallyl alcohol y-Phenylallyl alcohol 3-Phenyl-2-propenol 3-Phenyl-2-propen-1-ol Styrone Styryl alcohol Styryl carbinol... [Pg.956]

Synonyms Methyl styryl carbinol Uses Synthetic flavoring agent in foods and pharmaceuticals cigarette additive... [Pg.3311]

Styryl alcohol Styryl carbinol. See Cinnamyl alcohol... [Pg.4243]

In the same context, Livingston s group has studied the efficiency of a ruthenium p-cymene catalyst combined with Novozym 435 in the presence of a number of different bases for the DKR of allylic alcohols. Using this method, the DKR of methyl styryl carbinol, performed in the presence of a base such as... [Pg.198]

Acetylpyridazine and pyridazine-4-carbaldehyde are reduced with sodium borohydride to the corresponding carbinols (299 R = H or Me). ° Pyrid-azine-4-carbaldehyde (228 R = H) is prepared by oxidation of 4-styryl-pyridazine (227), obtained by condensation of 4-methylpyridazine with benzaldehyde." A similar procedure can be applied to prepare the 3-aldehyde, which can be obtained also from the corresponding carbinol by oxidation with manganese dioxide. With sodium in liquid ammonia under Birch reduction conditions halopyridazines are dehalogenated. ° ... [Pg.423]

In contrast cyclization and dcsilylation of 5, in which the phcnylcthynylsilyl group is linked to the 3 /3-hydroxyl group of a phcnylsclcnoglucosidc, provides the /3-C-glucosidc 6. The styryl group of 4 and 6 is useful as such and as a precursor of an aldehyde or a carbinol. Note that a free hydroxy group is liberated in this cyclization and can be useful for subsequent transformation. [Pg.77]

Benzylic Reactivity. 2,5-Dimethyl-3,4-dinitrothiophen has been condensed with aromatic aldehydes to give 3,4-dinitro-2,5-distyryl-thiophens. " An improved synthesis of 3-nitro-2-styryl-thiophens involves bromination of 3-methyl-2-nitrothiophen with A-bromosuccinimide, followed by a modified Wit-tig reaction. From 2,5-di(chloromethyl)thiophen, the phosphonate was prepared by the Arbusov reaction, which was used for the preparation of 2,5-distyryl-thiophens. Trichloromethyl(thienyl)carbinols have been converted into the corresponding fluoro-derivatives through the reaction with phenyl-tetrafluorophosphorane. The liquid-phase catalytic oxidation of phenyl-(2-thienyl)methane in acetic acid in the presence of cobalt(ll) acetate and sodium bromide has been investigated. ... [Pg.87]

In certain very limited cases the 750 cm" band shows splitting into a group of weaker bands at the same frequency. This occurs in the cw-forms of phenyl propenyl carbinol and styryl methyl carbinol [37], although the trans forms have only a single band of normal position and intensity. The reasons for this are not known, but it may be connected with steric interferences in the cis-compounds. Benzoyl derivatives also give rise to distortions in this region. The 750 cm" band is not seen in the Raman spectrum and the 690 cm" band appears only weakly. [Pg.87]

Vinylbenzyl alcohol (acetate) 2-(4-Vinylphenyl)ethanol (acetate) 4-Vinylbenzoic acid (methyl ester) 1,3-Diethyl-4-vinylbenzene 2-Nitro-4-vinylthiophenol Methylthio(4-vinylphenyl) 2-Nitro-4-vinylphenol 4-Chloromethylstyrene 4-Methoxystyrene Diphenyl(4-vinylphenyl)carbinol 4-Vinylbromo(iodo)benzene Sugar-(4-vinylbenzoate) Sugar-(4-vinylbenzenesulfonate) 2-p-Styryl-4,5-bistosyloxymethyl-1,4-dioxane... [Pg.25]

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