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4- tert-Butylcyclohexyl acetate

C12H20O4 diethyl cis-1,4-cyclohexanedicarboxylate 116724-15-3 543.32 48.061 2 24725 C12H2202 2-tert-butylcyclohexyl acetate 88-41-5 508.57 44.708 2... [Pg.515]

A portion of the H NMR spectrum (300 MHz, CDCI3) of commercially available 2-tert-butylcyclohexyl acetate (a mixture of cis/trans isomers) is reproduced here. The resonances shown in the expansion correspond to the proton indicated in bold on the structure. Which diastereomer is the major component, and which is the minor component ... [Pg.422]

Figure 24 Total ion chromatograms of washing powder. (A) SAFE versus (B) SDE. Key 1, Prenyl acetate 2, cw-3-Hexenyl acetate 3, 2-terL-Butylcyclohexyl acetate (cis-Agrumex) 4, 2-tert.-Butylcyclohexyl acetate (trans-Agnunex) 5, 1-Phenylethyl acetate 6, Geranyl acetate 7, Verdyl acetate. Figure 24 Total ion chromatograms of washing powder. (A) SAFE versus (B) SDE. Key 1, Prenyl acetate 2, cw-3-Hexenyl acetate 3, 2-terL-Butylcyclohexyl acetate (cis-Agrumex) 4, 2-tert.-Butylcyclohexyl acetate (trans-Agnunex) 5, 1-Phenylethyl acetate 6, Geranyl acetate 7, Verdyl acetate.
Esters of steroid alcohols display the usual order of reactivity according to the acyl group e,g. acetate > benzoate [6]), but the wide range of reactivities for the same acyl group e.g, acetate) must be steric in origin. The effect of conformation is shown by the relative rates of hydrolysis of trans- (3) and m-4-tert"butylcyclohexyl acetates (4) [y]. The equatorial... [Pg.263]

C12H20O2 linalyl acetate 115-95-7 505.75 44.437 2 24710 C12H2202 4-tert-butylcyclohexyl acetate 32210-23-4 508.57 44.708 2... [Pg.515]

C12H22O2, Mr 189.30, mp (pure cis isomer) 34.5-35.4 °C commercial product 0.938-0.944, nfj 1.4500-1.4560 this compound does not occur in nature and exists in cis and trans forms. Pure 2-cis-tert-butylcyclohexyl acetate is a crystalline solid, with a fruity, agrumen-like odor. The commercial product is a colorless liquid and consists of a mixture of cis and trans isomers, which contains 60- 95 % of the cis ester. With an increasing percentage of the trans isomer, the odor becomes more woody-camphory. [Pg.99]

Acetic acid, (4-tert-butylcyclohexyl) ester A13-36523 4-t-Butylcyclohexyl acetate 4-tert-Butyl cyclohexyl acetate 4-tert-Butylcyclohexanol acetate 4-tert-Butylhexahydrophenyl acetate Cyclohexanol, 4-(1,1-dimethylethyl)-, acetate Cyclohexanol, 4-tert-butyl-, acetate Cyclohexanol, 4-tert-butyl-, acetate (SCI) EINECS 250-964-9 NSC 163103 p-tert-Butyl cyciohexyl acetate p-tert-Butylcyclohexyl acetate Vertenex,... [Pg.92]


See other pages where 4- tert-Butylcyclohexyl acetate is mentioned: [Pg.91]    [Pg.277]    [Pg.99]    [Pg.297]    [Pg.297]    [Pg.91]    [Pg.91]    [Pg.92]    [Pg.277]    [Pg.277]    [Pg.99]    [Pg.297]    [Pg.297]    [Pg.297]    [Pg.297]    [Pg.92]    [Pg.367]    [Pg.421]    [Pg.198]    [Pg.163]   
See also in sourсe #XX -- [ Pg.91 ]

See also in sourсe #XX -- [ Pg.99 ]




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