Phenyl heptyl alcohol

Of these phenyl-amyl alcohol has a pleasant, but somewhat evanescent lemon-like odour phenyl-hexyl alcohol has a very similar odour to this and phenyl-heptyl alcohol has a slight, but extremely agreeable odour [Pg.129]

KETONES AND ALCOHOLS FROM ORGANOBORANES 1. PHENYL HEPTYL KETONE 2. 1-HEXANOL ... 

KETONES AND ALCOHOLS FROM ORGANOBORANES 1. PHENYL HEPTYL KETONE 2. HEX-ANOL 3. 1-OCTANOL,53, 77 Ketones, Clemmensen reduction of, 53, 89... 

Ethyl malonate Heptyl alcohol Phenyl acetate Benzyl methyl ether Phenetole Dimethylaniline... 

Acetic acid Acetone L-Camphor Caprolactam 2,2-Dimethylpropanol Ethylcellulose Ethylene 2-(5-Ethyl-2-pyridyl)ethyl acrylate Heptyl alcohol N-Isopropyl-N -phenyl-p-phenylenediamine Levulinic acid Nonanoic acid Rosin plastic mfg., cellulose propionate Propionic acid plastic pipe Polypropylene plastic resins Cobalt phosphate (ous) plastic wood s-Amyl acetate... 

Heptane Heptyl alcohol Indole Styrene Acetophenone Benzyl formate Methyl benzoate Phenyl acetate Methyl salicylate Ethylbenzene m-Xylene o-Xylene p-Xylene... 

Heptyl alcohol Acetophenone Methyl benzoate Phenyl acetate Benzyl methyl ether Phenethyl alcohol... 

A range of different functional groups has been introduced into the V-position of the C3 side chain, as shown in Table 6.10. A number of different functionalities were shown to be tolerated in this position, with lipophilic groups such as methyl and dithiolane being preferred over polar groups such as ketones and alcohols. Ketone (118) had similar CBi receptor affinity to the unfunctionalised -heptyl compound (84), while alcohol (120) had lower affinity. The phenyl ketone (119) had lower CBi receptor affinity than the simple benzyl-substituted compound (116), but higher CB2 affinity, with about 12-fold selectivity for CB2 over CBi. 

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