Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Isopropyl-5-methyl-cyclohexanol

Synonyms cas sp-ts-i hexahydrothymol 2-isopropyl-5-methyl-cyclohexanol p-menthan-3-ol ... [Pg.199]

Menthol = (-)-(lJf,25, 5J )-2-Isopropyl-5-methyl-cyclohexanol (+)-Menthol = (+)-(15,2J ,5 S)-2-Isopropyl-5-methyl-cyclohexanoI... [Pg.147]

Synonyms Cyclohexanol, 2-isopropyl-5-methyl- Cyclohexanol, 5-methyl-2-(1-methylethyl)- Hexahydrothymol 2-lsopropyl-5-methylcyclohexanol 3-p-Menthanol p-Menthan-3-ol 5-Methyl-2-isopropylcyclohexanol 5-Methyl-2-isopropyl hexahydrophenol 5-Methyl-2-(1-methylethyl) cyclohexanol Peppermint camphor Racemic menthol Classification Diterpene alcohol Definition Alcohol obtained from diverse mint oils, Mentha spp. or prepared synthetically may be levorotatory (I-), from natural or syn. sources, or racemic (dl-)... [Pg.2521]

The first successful industrial production of ( )-menthol was based on 3-methyl-phenol 2, which was transformed in two steps into 2-isopropyl-5-methyl cyclohexanol 4, i.e., into the menthol skeleton (Scheme 9.1) [10]. This structure has three stereogenic centres and therefore 2 = 8 stereoisomers. The inherent beauty of this process resides in the complete regioselectivity of isopropylation, controlled stereoelectrorrically by the two substituents oti the aromatic ring, and the high diastereoslectivity of hydrogenation to the all-trans product, one of three possible racemic diastereomers. [Pg.118]

EINECS 203-468-6, see Ethylenediamine EINECS 203-470-7, see Allyl alcohol EINECS 203-472-8, see Chloroacetaldehyde EINECS 203-481-7, see Methyl formate EINECS 203-523-4, see 2-Methylpentane EINECS 203-528-1, see 2-Pentanone EINECS 203-544-9, see 1-Nitropropane EINECS 203-545-4, see Vinyl acetate EINECS 203-548-0, see 2,4-Dimethylpentane EINECS 203-550-1, see 4-Methyl-2-pentanone EINECS 203-558-5, see Diisopropylamine EINECS 203-560-6, see Isopropyl ether EINECS 203-561-1, see Isopropyl acetate EINECS 203-564-8, see Acetic anhydride EINECS 203-571-6, see Maleic anhydride EINECS 203-576-3, see m-Xylene EINECS 203-598-3, see Bis(2-chloroisopropyl) ether EINECS 203-604-4, see 1,3,5-Trimethylbenzene EINECS 203-608-6, see 1,3,5-Trichlorobenzene EINECS 203-620-1, see Diisobutyl ketone EINECS 203-621-7, see sec-Hexyl acetate EINECS 203-623-8, see Bromobenzene EINECS 203-624-3, see Methylcyclohexane EINECS 203-625-9, see Toluene EINECS 203-628-5, see Chlorobenzene EINECS 203-630-6, see Cyclohexanol EINECS 203-632-7, see Phenol EINECS 203-686-1, see Propyl acetate EINECS 203-692-4, see Pentane EINECS 203-694-5, see 1-Pentene EINECS 203-695-0, see cis-2-Pentene EINECS 203-699-2, see Butylamine EINECS 203-713-7, see Methyl cellosolve EINECS 203-714-2, see Methylal EINECS 203-716-3, see Diethylamine EINECS 203-721-0, see Ethyl formate EINECS 203-726-8, see Tetrahydrofuran EINECS 203-729-4, see Thiophene EINECS 203-767-1, see 2-Heptanone EINECS 203-772-9, see Methyl cellosolve acetate EINECS 203-777-6, see Hexane EINECS 203-799-6, see 2-Chloroethyl vinyl ether EINECS 203-804-1, see 2-Ethoxyethanol EINECS 203-806-2, see Cyclohexane EINECS 203-807-8, see Cyclohexene EINECS 203-809-9, see Pyridine EINECS 203-815-1, see Morpholine EINECS 203-839-2, see 2-Ethoxyethyl acetate EINECS 203-870-1, see Bis(2-chloroethyl) ether EINECS 203-892-1, see Octane EINECS 203-893-7, see 1-Octene EINECS 203-905-0, see 2-Butoxyethanol EINECS 203-913-4, see Nonane EINECS 203-920-2, see Bis(2-chloroethoxy)methane EINECS 203-967-9, see Dodecane EINECS 204-066-3, see 2-Methylpropene EINECS 204-112-2, see Triphenyl phosphate EINECS 204-211-0, see Bis(2-ethylhexyl) phthalate EINECS 204-258-7, see l,3-Dichloro-5,5-dimethylhydantoin... [Pg.1482]

The solvents most commonly employed are water, ethyl and methyl alcohol, ether, benzene, petroleum ether, acetone, glacial acetic acid also two or three solvents may be mixed to get the desired effect as described later. If you still cannot dissolve the compound, try some of these chloroform, carbon disulfide, carbon tetrachloride, ethyl acetate, pyridine, hydrochloric acid, sulfuric acid (acids are usually diluted first), nitrobenzene, aniline, phenol, dioxan, ethylene dichloride, di, tri, tetrachloroethylene, tetrachloroethane, dichloroethyl ether, cyclohexane, cyclohexanol, tetralin, decalin, triacetin, ethylene glycol and its esters and ethers, butyl alcohol, diacetone alcohol, ethyl lactate, isopropyl ether, etc. [Pg.10]

Nitroglycol, Nitrocellulose, Potassium nitrate. Flour Phosphorus trichloride. Aluminum chloride. Methyl chloride. Methylene chloride. Hydrochloric acid. Sodium fluoride, Cyclohexanol, Silica gel. Isopropyl ether. Toluene... [Pg.104]

Problem 14.55 Prepare the following ethers starting with benzene, toluene, phenol (C H OH), cyclohexanol, any aliphatic compound of three C s or less and any solvent or inorganic reagent a) dibenzyl ether, b) di-/i-butyl ether, (c) ethyl isopropyl ether, d) cyclohexyl methyl ether, (e) p-nitrophenyl ethyl ether, (/) divinyl ether (g) diphenyl ether. <... [Pg.311]

Chemicals and Standard Solutions. Cyclohexanone, cyclohexanol, 1,3,5-trichlorobenzene, 1,2,4-trichlorobenzene, phenol, 4-methylphenol, 4-chloro-phenol, 1,2,3,4-tetrahydroisoquinoline, 1-chlorohexane, 1-chlorododecane, and 1-chlorooctadecane were obtained from Aldrich. Acetone, tetrahydrofuran, ethyl acetate, toluene, dimethyl sulfoxide, and methanol were obtained from J. T. Baker. Distilled-in-glass isooctane, methylene chloride, ethyl ether, and pentane were obtained from Burdick and Jackson. Analytical standard kits from Analabs provided methyl ethyl ketone, isopropyl alcohol, ethanol, methyl isobutyl ketone, tetrachloroethylene, dodecane, dimethylformamide, 1,2-dichlorobenzene, 1-octanol, nitrobenzene, 2,4-dichlorophenol, and 2,5-dichlorophenol. All chemicals obtained from the vendors were of the highest purity available and were used without further purification. High-purity water... [Pg.356]

Monocyclic monoterpenes include the fully saturated menthol (5-methyl-2-isopropyl-cyclohexanol) (C6) (peppermint smell), the fully unsaturated analogue thymol (5-methyl-2-isopropylphenol) (G6) (smell of thyme) and the partially unsaturated a-terpinene (5,6-dihydro-4-isopropyltoluene) (G6) (lemon odour). Variants derive from different degrees of unsaturation and substitution and from different functional groups (e.g. alkyl, hydroxyl, aldehyde, peroxy and keto groups). [Pg.35]

SYNS CYCLOHEXANOL, 2-ISOPROPYL-5-METHYL- FEMA No. 2665 HEXAHYDROTHYMOL 2-ISOPROPYL-5-METHYLCYCLOHEXANOL P-MENTHAN-3-OL 1-iMENTHOL 5-METHYL-2-(l-METHYLETHYL)CY-CLOHEXANOL PEPPERMINT CAMPHOR TRA-KILL TRACHEAL MITE KILLER... [Pg.866]

SYNS FEMA No. 2665 4-ISOPROPYL-l-METHYL-CYCLOHEXAN-3-OL dl-3-p-MENTHANOL 3-p-MENTHOL MENTHOL racemic MENTHOL racemique (FRENCH) 5-METHYL-2-(l-METHYLETHYL)-CYCLOHEXANOL (l-0,2-P,5-a)... [Pg.866]

SYNS FEMA No. 2668 1-2-ISOPROPYL-5-METHYL-CYCLOHEXAN-l-OL ACETATE (-)-MENTHYL ACETATE 1-MENTHYL ACETATE (FCC) 1-p-MENTH-3-YL ACETATE (R-(la,2P,5a))-5-METHYL-2-(l-METHYLETHYL)-CYCLOHEXANOL ACETATE (9CI)... [Pg.867]

HYDROPEROXYCYCLOHEXYL)DIOXY)- see CPC300 CYCLOHEXANOL, p-ISOPROPYL- see 100300 CYCLOHEXANOL, 2-ISOPROPYL-5-METHYL- see MCF750... [Pg.1600]

Cyclohexanol. See Cyclohexanol Cyclohexanol acetate. See Cyclohexyl acetate Cyclohexanol, 4-t-butyl- Cyclohexanol, 4-(1,1-dimethylethyl)-. See 4-t-Butylcyclohexanol Cyclohexanol, 2-(1,1-dimethylethyl)-, acetate. See 2-t-Butylcyclohexyl acetate Cyclohexanol formate. See Cyclohexyl formate Cyclohexanol, 1 -((1-hydroperoxycyclohexyl) dioxy)-. See Cyclohexanone peroxide Cyclohexanol, 4,4 -isopropylidenedi-. See Bisphenol A, hydrogenated Cyclohexanol, 2-isopropyl-5-methyl-. See Menthol... [Pg.1120]

See other pages where Isopropyl-5-methyl-cyclohexanol is mentioned: [Pg.59]    [Pg.245]    [Pg.266]    [Pg.515]    [Pg.516]    [Pg.59]    [Pg.245]    [Pg.266]    [Pg.515]    [Pg.516]    [Pg.1570]    [Pg.212]    [Pg.1637]    [Pg.1570]    [Pg.403]    [Pg.97]    [Pg.1570]    [Pg.1604]    [Pg.2523]    [Pg.2534]    [Pg.2568]    [Pg.645]   
See also in sourсe #XX -- [ Pg.2 , Pg.199 ]



SEARCH



Cyclohexanol

Methyl cyclohexanol

© 2024 chempedia.info