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Ethyl undecanoate

Ethyl Tuads Rodform, Ethyl Tuex . See Tetraethylthiuram disulfide Ethyl undecanoate CAS 627-90-7... [Pg.1780]

Ethyl undecylate. See Ethyl undecanoate Ethyl undecylenate Ethyl undecylenoate. See Ethyl 10-undecenoate... [Pg.1781]

Ethyl-3-phenylpropionate Ethyl propionate Ethyl pyruvate Ethyl salicylate Ethyl sorbate Ethyl tiglate Ethyl undecanoate Ethyl 10-undecenoate Ethyl valerate Ethyl vanillin Eucalyptol Eugenol Eugenyl acetate Eugenyl benzoate ,Eugenyl formate Farnesol d-Fenchone l-Fenchone Fenchyl alcohol Formic acid... [Pg.5289]

Ethyl sorbate Ethyl undecanoate Ethyl vanillin Formic acid Furfuryl thioacetate Geranium maculatum oil a-D-Glucose pentaacetate Guaiol acetate Heptyl crotonate Heptyl isobutyrate Heptyl valerate Hexanal propylene glycol acetal cis-3-Hexenyl anthranilate cis-3-Hexenyl benzoate cis-3-Hexenyl crotonate cis-3-Hexenyl hexanoate 3-Hexenyl isovalerate cis-3-Hexenyl phenylacetate cis-3-Hexenyl senecioate Hexenyl-cis-3-valerate Hexyl alcohol Hexyl 2-furoate Hexyl lactate Hexyl nicotinate Hexyl phenylacetate Hexyl valerate Hydroxycitronellal residue Hydroxylamine sulfate 5-Hydroxy-4-octanone y-lonone... [Pg.5318]

Amyl octanoate Decyl propionate Ethyl undecanoate Isoamyl octanoate Isobutyl pelargonate Methyl laurate Octyl isovalerate Octyl neopentanoate... [Pg.7084]

Cetene-1 Ethanol Ni/Nilj Mixture of ethyl undecanoates 61 [525]... [Pg.109]

The mesogenic units with methylenic spacers were prepared by reacting the sodium salt of either 4-methoxy-4 -hydroxybiphenyl or 4-phenylphenol with a bromoester in DMF at 82° C for at least 4 hours in the presence of tetrabutylammonium hydrogen sulfate (TBAH) as phase transfer catalyst. In this way, ethyl 4-(4-oxybi-phenyl)butyrate, ethyl 4-(4-methoxy-4 -oxybiphenyl)butyrate, ethyl 4-(4-oxybiphenyl)valerate, ethyl 4-(4-methoxy-4 -oxybiphenyl)-valerate, n-propyl 4-(4-oxybiphenyl)undecanoate and n-propyl 4-(4-methoxy-4 -oxybiphenyl)undecanoate were obtained. These esters were hydrolyzed with base and acidified to obtain the carboxylic acids. The corresponding potassium carboxylates were obtained by reaction with approximately stoichiometric amounts of potassium hydroxide. Experimental details of these syntheses were described elsewhere (27). [Pg.102]

See other pages where Ethyl undecanoate is mentioned: [Pg.26]    [Pg.226]    [Pg.251]    [Pg.76]    [Pg.179]    [Pg.382]    [Pg.523]    [Pg.583]    [Pg.634]    [Pg.762]    [Pg.378]    [Pg.379]    [Pg.1090]    [Pg.370]    [Pg.371]    [Pg.1075]    [Pg.1146]    [Pg.1740]    [Pg.5283]    [Pg.6153]    [Pg.178]    [Pg.357]    [Pg.358]    [Pg.1025]    [Pg.413]    [Pg.414]    [Pg.1297]    [Pg.404]    [Pg.405]    [Pg.1163]    [Pg.401]    [Pg.402]    [Pg.1187]    [Pg.412]    [Pg.413]    [Pg.1294]    [Pg.370]    [Pg.371]    [Pg.1059]    [Pg.2138]    [Pg.114]    [Pg.73]    [Pg.257]    [Pg.461]   
See also in sourсe #XX -- [ Pg.560 ]

See also in sourсe #XX -- [ Pg.76 ]



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Undecanoate

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