Cyclohexyl propionate

Cyclohexyl acetate Cyclohexyl propionate Cylohexyl salicylate Dicyclopentadienyl... 

Cyclohexyl propan-1-ol 2-Cyclohexyl-1-propanol. See Cyclohexylpropanol Cyclohexyl propionate CAS 6222-35-1... 

Cyclohexaneacetic acid Cyclohexanecarboxylic acid Cyclohexanone Cyclohexyl acetate Cyclohexyl anthranilate Cyclohexyl butyrate Cyclohexyl cinnamate Cyclohexylethyl acetate Cyclohexyl formate Cyclohexyl isovalerate Cyclohexyl propionate Cyclopentanethiol Cyclopentanone p-Cymene trans-trans-2,4-Decadienal... 

Cyclohexyl formate Cyclohexyl isobutyrate Cyclohexyl propionate Decyl butyrate ... 

C9H16O2 Allyl caproate Allyl 2-ethyl butyrate Butyl tiglate Cyclohexyl propionate... 

Vinylcyclo- hexene-3 Pd(P(C6H5)3)2Cl2/HCl Isomeric (carboxy-cyclohexyl)-propionic acids [469]... 

C21H40O2 3-cyclohexyl-propionic acid dodecyl ester 102899-46-7... 

M-Butyl formate. Ethyl iso-butyrate IsO -butyl acetate Ethyl butyrate -Propyl propionate Iso-amyl formate, -But> l acetate Iso-propyl butyrate Iso-butyl propionate n-Propyl -butyrate -Butyl propionate Iso-butyl isobutyrate Ethyl lactate Iso-butyl butyrate Cycloheicyl formate -Butyl -butyrate Iso-propyl lactate. Cyclohexyl acetate Diethyl oxalate Di-iao-propyl oxalate... 

METHYL ISOBUTYL KETONE n-PENTYL FORMATE n-BUTYL ACETATE sec-BUTYL ACETATE tert-BUTYL ACETATE ETHYL n-BUTYRATE ETHYL ISOBUTYRATE ISOBUTYL ACETATE n-PROPYL PROPIONATE CYCLOHEXYL PEROXIDE DIACETONE ALCOHOL 2-ETHYL BUTYRIC ACID n-HEXANOIC ACID 2-ETHOXYETHYL ACETATE HYDROXYCAPROIC ACID PARALDEHYDE... 

Apple Allyl butyrate, cyclohexylvalerate, isovalerate, propionate Benzyl isovalerate Butyl isovaleratc. valerate Cinnamyl formate, isobuiyrate. isovaleraie Citronellyl isovaleraie Cyclohexyl acetate, butyrate, isovalerate Ethyl isovalerate, valerate Isopropyl acetate, valerate 2-Methylallyl butyrate Methyl butyrate Terpenyl isovaleraie... 

Banana Cyclohexyl acetate, butyrate, propionate Ethyl valerate. 

Cherry Allyl ben/oale. Anisyl butyrate, propionate. Cyclohexyl cinnamute. formate Methyl anthranilme Rhodinyl formate Tetrahydrogeraniol Tolualdehyde u>./ . pi. 

Currant Cyclohexyl butyrate Guaiol acetate (black currant) Linalyl acetate, isobutyrate, propionate (black currant) Methyl ionone Methyl propionate (black currant). 

Nevertheless, diastereomeric product 26 was used to test the validity of the Claisen approach. Thus, esterification of 26 with propionic anhydride offered the requisite ester 15 along with the inseparable diastereomer 15a (1 1 ratio). Kinetic deprotonation of the mixture of 15/15a was effected with lithium N-cyclohexyl-lV-isopropylamide (LICA) and, upon warming to room temperature, Ireland-Claisen... 

Oxo-cyclohexyl)phenyl]propionic acid Hydroxylamine hydrochloride... 

Oxocyclohexyl)phenyl]propionic acid (4.0 g 16.2 mmoles) is dissolved in 1 N sodium hydroxide (55 ml) and treated with hydroxylamine hydrochloride (2.22 g 32 mmoles) during 24 h at room temperature. The gummy precipitate formed on acidification is converted to the sodium salt in aqueous solution which is then evaporated to dryness. The residue is dissolved in methanol or ethanol to remove an insoluble. After evaporating off the alcool, the sodium salt is again dissolved in water and converted to the acid which is crystallized from water-methanol (1 1), to give 3.0 g (yield 70%) of 2-[4-(3 -hydroxyimino-cyclohexyl)phenyl]propionic acid, melting point... 

To the (2S)-2-benzyl-3-(l-methylpiperatin-4-ylsulfonyl)propionic acid (1.0 g, 3.064 mmol), the H-L-(4-thiazolyl)Ala amide of (2S,3R,4S)-2-amino-l-cyclohexyl-3,4-dihydroxy-6-methylheptane (1.11 g, 2.792 mmol), and 1-hydroxybenzotriazole (1.022 g, 7.563 mmol) in dimethylformamide (20 ml) was added N-methylmorpholine (0.35 ml, 3.2 mmol). The mixture was cooled to -23°C and treated with l-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.760 g, 3.96 mmol). After 2 h at -23°C and 14 h at room temperature, the reaction was poured into saturated NaHC03 solution (100 ml) and extracted into ethyl acetate (2x50 ml) which was washed with water (2x50 ml) and brine (50 ml) and then was dried over Na2S04 and evaporated to afford 1.94 g. Recrystallization from ethanol (15 ml)/hexane (90 ml) afforded 1.55g (79%) of (2S)-2-benzyl-3-(l-methylpiperazin-4-ylsulfonyl)propionyl-(L)-(4-thiazolyl)Ala-amide of (2S,3R,4S)-2-amino-l-cyclohexyl-3,4-dihydroxy-6-methylheptane as a white solid, melting point 169°-170°C. 

RX. n-butyl bromide n-dodecanyl iodide cyclohexyl iodide ethyl bromo acetate methyl 2,3-di-O-acetyl-4-O-benzoyl-6-bromo-6-deoxy-ot-D-glucopyranoside methyl 2,3,4-tri-0-acetyl-6-deoxy-6-iodo-0 -D glucopyranoside l,2 3,4-di-0-isopropylidene-6-deoxy-6-iodo-a-D-galactopyranose methyl 2(R)-[(tert-butoxycarbonyl)amino]-3-iodo-propionate cyclic bis(trifluoromethyl)oxazolidinone bromide. 

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). ... 

C12H15CIO 2-chloro-4-cyclohexyl phenol 3964-61-2 15.00 1.1600 1 24252 C12H1603 2,2-dimethyl-3-hydroxy-3-(p-tolyl)propionic. .. 22. To5 2 o... 

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