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Cyclohexyl Alcohol

A) (i) Distillate. Test for the alcohol. e.g., methyl, ethyl, benzyl, or cyclohexyl alcohol. [Pg.413]

Cyclohexanol Cyclohexyl alcohol 94 QHi,0 Methyl teti-hutyl ether 107 C5H12O... [Pg.99]

Chemical Designations - Synonyms Adronal Anol Cyclohexyl Alcohol Hexalin Hexahydrophenol Hydroxycyclohexane Chemical Formula (CH jCHOH. [Pg.99]

Monocyclohexyl phosphates and phosphonates can be cleaved by a two-step process in which the ester is treated with an epoxide such as propylene oxide to form another ester, which, upon treatment with base, releases the cyclohexyl alcohol. ... [Pg.671]

Synonyms Adronal Adronol AI3-00040 Anol BRN 0906744 CCRIS 5896 CXL Cyclohexyl alcohol EINECS 203-630-6 Hexahydrophenol Hexalin Hydralin Hydrophenol Hydroxycyclo-hexane Naxol NSC 403656 NSC 54711. [Pg.329]

Cyclohexene, see Cyclohexene Cyclohexyl alcohol, see Cyclohexanol Cyclohexyl ketone, see Cyclohexanone Cyclohexylmethane, see Methylcyclohexane Cyclopenta-1,3-diene, see Cyclopentadiene 1,3-Cyclopentadiene, see Cyclopentadiene Cyclopentamethylene, see Cyclopentane Cyclopenta[(/,e]naphthalene. see Acenaphthylene Cyclopenten, see Cyclopentene Cyclopentenyl, see Cyclopentene... [Pg.1473]

Ketals of acetone and cyclohexanone with methyl, butyl, isopropyl and cyclohexyl alcohols are hydrogenolyzed to ethers and alcohols by catalytic hydrogenation. While platinum and ruthenium are inactive and palladium only partly active, 5% rhodium on alumina proves to be the best catalyst which, in the presence of a mineral acid, converts the ketals to ethers and alcohols in yields of 70-100% [933]. [Pg.130]

CYCLOHEXANOL Hexalin, Adronal, Anol, Cyclohexyl Alcohol Combustible Liquid 1 2 0... [Pg.99]

Alcohol inversion. Elimination competes with S, 2 substitution in the inversion of secondary alcohols by the Mitsunobu reaction or by reaction of mesylates with cesium propionate or cesium acetate. Elimination in the inversion of cyclopentyl and cyclohexyl alcohols can be largely suppressed by reaction of the mesylate with cesium acetate (excess) and a catalytic amount of l8-crown-6 in refluxing benzene. Even inversion of an ally lie alcohol can be effected in moderate yield under these conditions (equation I). ... [Pg.109]

Cyclohexanol Cyclohexyl alcohol 94 CeHi20 Methyl butyl ether 107 C4H13O... [Pg.96]

SYNS ADRONAL ANOL CICLOESANOLO (ITALIAN) CYCLOHEXYL ALCOHOL CYKLOHEKSANOL (POLISH) D HEXAHYDROPHENOL HEXALIN HYDRALIN HYDROPHENOL HYDROXYCYCLOHEXANE NAXOL... [Pg.402]

CYCLOHEXYL ACETATE see CPFOOO CYCLOHEXYL ALCOHOL see CPB750 CYCLOHEXYLAMIDOSULPHURIC ACID see CPQ625 CYCLOHEXYLAMINE see CPF500 CYCLOHEXYLAACNESULPHONIC ACID see CPQ625 N-CYCLOHEXYL-2-... [Pg.1600]

Without rigorous control of temperature and reaction time, a mixture of the co-monoester, the diester, and the dicarboxylic acid is formed. Moreover, the presence of the residual unreacted cyclohexyl alcohol hinders the isolation of the desired compound. Therefore, complete removal of the alcohol is required.)... [Pg.250]

Cyclohexyl Alcohol Cyclohaxylamine Cymene Ip-) 23 f 7 7 7 jhat ratialahi ii. c w... [Pg.13]

Cyclohexyl Alcohol cydohexanol 30 5 partially soluble in reagent Eval 40 inol% VA conlsrit... [Pg.133]

Cyclohexyl Alcohol 23 6 Si chg.afisrkiAg aipos.. cauiicn 9 high lamp./conc Aiiiad Sig. Capror)... [Pg.312]

Cyclohexanone Cyclohexyl Alcohol Diesel Fuels Dimethyl an nine DIoxane (p-) Epichlorohydrin Ethyl Acetate Ethylene Chloride... [Pg.465]

Cyclohexyl Alcohol Cyclopropane Deep Frying Oil Degreasing Cleaners Detergents DIbutyl Fhthalate Dfchlorobenzene... [Pg.747]

Cyclohexyl Alcohol 108-93-0 Dichlorodiethyl Ether 27753-54-4 Diisopropyl Benzene 25321-09-9... [Pg.1074]

A new polymer-bound reagent system for the efficient oxidation of primary alcohols to aldehydes and of secondary alcohols to ketones in the presence of a catalytic amount of 2,2,6,6-tetramethyl-l-piperidonoxyl (TEMPO) has been described [102]. Work-up of this heavy metal free oxidation is achieved by simple filtration followed by removal of the solvent. Benzyl alcohol was oxidized in 94% yield. The more demanding cyclohexyl alcohol was converted into cyclohexanone in 96 % yield. [Pg.492]

Then the solid V4O9 (20 g) was suspended in 100 g of various fresh alcohols (isopropyl alcohol, isobutyl alcohol, 2- butyl alcohol, 2- methyl-1- butyl alcohol, cyclohexyl alcohol or 2-ethyl-1-hexyl alcohol). The suspension was heated until 383K. (In the cases of isopropyl alcohol and 2- butyl alcohol, the suspension was heated until reflux.) Then, here added an ortho-H3PO4 (18.2 g) in the same alcohol (7.2 g) dropwisely for 30 minutes. The ratio of P to V was 1.13 for preparation of the precursor. After H3PO4 addition, this condition was kept for 5 hours (in the case of isopropyl alcohol, for 24 hours). Then the obtained slurry was filtered. Thus obtained solid was washed with acetone and was dried at 313 K for 15 hours. [Pg.836]

See other pages where Cyclohexyl Alcohol is mentioned: [Pg.264]    [Pg.159]    [Pg.38]    [Pg.181]    [Pg.1173]    [Pg.220]    [Pg.175]    [Pg.374]    [Pg.25]    [Pg.431]    [Pg.264]    [Pg.395]    [Pg.40]    [Pg.146]    [Pg.167]    [Pg.212]    [Pg.268]    [Pg.289]    [Pg.330]    [Pg.342]    [Pg.518]    [Pg.685]    [Pg.1084]    [Pg.627]   
See also in sourсe #XX -- [ Pg.99 ]

See also in sourсe #XX -- [ Pg.58 , Pg.78 ]

See also in sourсe #XX -- [ Pg.195 ]

See also in sourсe #XX -- [ Pg.58 , Pg.78 ]

See also in sourсe #XX -- [ Pg.58 , Pg.78 ]

See also in sourсe #XX -- [ Pg.99 ]

See also in sourсe #XX -- [ Pg.185 ]

See also in sourсe #XX -- [ Pg.207 ]



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Alcohol cyclohexyl secondary

Cyclohexyl

Cyclohexyl-based Alcohols

Cyclohexylation

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