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Propanoate, cyclohexyl 2-

Scheme 8.54. The reaction of propanoyl chloride with cyclohexanol in the presence of pyridine to form cyclohexyl propanoate. Scheme 8.54. The reaction of propanoyl chloride with cyclohexanol in the presence of pyridine to form cyclohexyl propanoate.
Scheme 8.55. The attack of cyclohexanol onto protonated propanoic acid as an example of the addition of an alcohol to the carbonyl of a protonated carboxylic acid. After reversible loss of water, the ester cyclohexyl propanoate resnlts. Scheme 8.55. The attack of cyclohexanol onto protonated propanoic acid as an example of the addition of an alcohol to the carbonyl of a protonated carboxylic acid. After reversible loss of water, the ester cyclohexyl propanoate resnlts.
Propanoic Acid 3-Cyclohexyl-2-fluoro- ElOb, 254 (NH2 - F) C,H,sFOj Butanoate ... [Pg.667]

Propanoate Ethyl 3-Cyclohexyl-2,2-difluoro-3-hydroxy- E10b2, 52 (Educl)... [Pg.687]

Propanoate Ethyl 3-Cyclohexyl-2-fiuoro-3-hydroxy- EI0b2, 52 (Educt)... [Pg.687]

ETHYL 4-CYCLOHEXYL-4-OXOBUTANOATE CYCLOHEXANEBUTANOIC ACID, Y-OXO-, ETHYL ESTER (54966-52-8), 65, 17 ETHYL CYCLOPROPYLPROPIOLATE, 66, 173,174 ETHYL (E,Z)-2,4-DECADIENOATE (3025-30-7), 66, 22, 23, 25, 28 Ethyl 3,4-decadienoate (36186-28-4), 66, 22, 28 Ethyl decanoate Decanoic acid, ethyl ester (110-38-3), 67,125 ETHYL DIETHOXYPROPANOATE PROPANOIC ACID, 3.3-DIETHOXY-,... [Pg.145]

Methyl-2-(l-methylethyl)cyclohexyl 2-hydroxy-propanoate [59259-38-0], /-mcnthyl lactate... [Pg.75]

Two novel aromatase inhibitors, designated FCE24786 (Af-cyclohexyl-2-(4-aminophenyl)propanamide (9)) and FCE24328 (cyclohexyl 2-(4-aminophen-yl)propanoate) have been described by workers from Farmitalia Carbo Erba... [Pg.263]

Phenoxy acid herbicides, sulfonyl ureas, quaternary ammonium derivatives (quats), and aryloxy propanoic acids are the main classes of compounds subjected to capillary zone electrophoresis (CZE). Triazines are also separated using nonaqueous CZE, while low pfCa characterized chlorotriazines require an ion-pair-like solubilization using cationic surfactants (tetradecylammonium bromide, dodecyltrimethyl-ammonium bromide). Chiral selectors are added in CZE for obtaining enantioselectivity. Chiral selectors used for herbicide enantiomeric discrimination are vancomycin, y-cyclodextrin, ethyl carbonate -cyclo-dextrin, cyclohexyl-alkyl-)S-D-maltoside, sulpropyl ether a-cyclodextrin, and hexakis(2,3-di-0-methyl)-a-cyclodextrin. [Pg.2072]

Table 5. Transition temperatures and phase assignments for a series of (R)- and (f ,S)-2- 4-[4-(frani-4-pentyl-cyclohexyl)benzoyloxy]phenoxy propanoates and a propanonitrile. Table 5. Transition temperatures and phase assignments for a series of (R)- and (f ,S)-2- 4-[4-(frani-4-pentyl-cyclohexyl)benzoyloxy]phenoxy propanoates and a propanonitrile.
See other pages where Propanoate, cyclohexyl 2- is mentioned: [Pg.972]    [Pg.1228]    [Pg.485]    [Pg.253]    [Pg.1087]    [Pg.245]    [Pg.1072]    [Pg.1142]    [Pg.160]    [Pg.160]    [Pg.653]    [Pg.654]    [Pg.870]    [Pg.1022]    [Pg.279]    [Pg.1294]    [Pg.1159]    [Pg.267]    [Pg.268]    [Pg.1184]    [Pg.278]    [Pg.279]    [Pg.1291]    [Pg.580]    [Pg.245]    [Pg.1056]    [Pg.239]    [Pg.686]    [Pg.686]    [Pg.419]   
See also in sourсe #XX -- [ Pg.263 ]



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2- Propano

2- propanoic

Cyclohexyl

Cyclohexylation

Propanoates

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