Geranyl ethyl ether

C12H20O2 5-methyl-2-(1 -methylvinyl)cyclohexanol aceta 57576-09-7 505.75 44.437 2 24695 C12H220 geranyl ethyl ether 40267-72-9 467.90 40.809 2... [Pg.515]

Ethoxy-3,7-dimethylocta-2,6-diene. See Geranyl ethyl ether... [Pg.1676]

CAS 56172-46-4 EINECS/ELINCS 260-027-0 Synonyms (E,E)-3,7-Dimethyl-2,6-octadienyl 2-butenoate Empirical C14H22O2 Properties M.w. 222.33 Toxicology TSCA listed Uses Fragrance in cosmetics Manuf./Distnb. Grau Aromatics http //www.grau-aromatics.de-, Jnterchim http //www.interchim. com Geranyl ethyl ether... [Pg.1876]

Behenyl hydroxyethyl imidazoline Schercozoline B 40160-92-7 Pentadoxynol-200 40267-72-9 Geranyl ethyl ether 40292-82-8 Neodecanoyl chloride 40372-72-3... [Pg.6522]

Behenyl hydroxyethyl imidazoline Schercozoline B 254-867-7 Geranyl ethyl ether 254-896-5... [Pg.6952]

Cyclododecanone 2-Dodecenal Epoxycyclododecane 2-Ethyl fenchol Geranyl ethyl ether 2-Heptylcyclopentanone... [Pg.7079]

CIC The weak juicy flavour is based on geraniol, geranyl acetate and neryl acetate in combination with linalyl ethyl ether and myrcenyl ethyl ether. The cold pressed peel oil has a high terpene content. Its flavour is dominated by citral, gamma-terpinene and alpha-pinene. Citral is recognized as a very important contributor to the fresh lemon character, although it decomposes within a few weeks in acidic soft drinks. [Pg.415]

A total synthesis of ethyl geranate (28) makes use of the addition of ethyl 4-bromo-3-methylbut-2-enoate (29) to the nickel carbonyl complex (30) of prenyl bromide. Geranyl acetate and the ethyl ether were made in a similar way. ... [Pg.15]

Linalool can be converted to geranyl acetone (63) by the CarroU reaction (34). By transesterification with ethyl acetoacetate, the intermediate ester thermally rearranges with loss of carbon dioxide. Linalool can also be converted to geranyl acetone by reaction with methyl isopropenyl ether. The linalyl isopropenyl ether rearranges to give the geranyl acetone. [Pg.421]

SYNS l-ETHOXY-3,7-DIMETHYL-2,6-OCTADIENE ETHYL GERANYL ETHER 2,6-OCTADIENE, 1-ETHOXY-3.7-DIMETHYL-... [Pg.691]

CAS 40267-72-9 EINECS/ELINCS 254-867-7 Synonyms 1 -Ethoxy-3,7-dimethylocta-2,6-diene Ethyl geraniol Ethyl geranyl ether... [Pg.1876]

Dihydromyrcenol Dihydromyrcenyl acetate Dimethyl benzenebutanol 2,4-Dimethyl-3-cyclohexene carboxaldehyde Dimethylcyclohexyl methyl ketone 4,8-Dimethyl-4,9-decadienal 5,9-Dimethyl-4,8-decadienal Ethyl acetoxyhexanoate Ethyl o-anisate Geranyl butyrate Geranyl formate Geranyl nitrile Greenyl acetate Hexahydrohexamethyl cyclopentabenzopyran Homolinalool Homolinalyl acetate Hydroxycitronellal Hydroxycitronellal dimethyl acetal Hydroxycitronellal methyl anthranilate Hydroxymethylheptyl methyl ketone Isoamyl phenethyl ether Isoamyl salicylate Isobornyl acetate 2-lsobutylquinoline a-Isomethylionone... [Pg.5329]

Linalool can be converted to geranyl acetone by the Carroll reaction (156). After transesterification with ethyl acetoacetate, the intermediate ester thermally rearranges with loss of carbon dioxide. Linalool can also be converted to geranyl acetone by reaction with methyl isopropenyl ether. The linalyl isopropenyl ether rearranges to give geranyl acetone. Geranyl acetone is an important intermediate in the synthesis of isophytol [505-32-8], famesol [106-28-5], and nerolidol [40716-66-3]. Isophytol is used in the manufacture of Vitamin E and thus linalool is a key intermediate in the synthesis of the latter. All of these reactions are shown in Fig. 8.55 in the section on nerolidol. [Pg.281]

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