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Propyl benzoates

The following liquids may be used (boiling points are given in parentheses) — chlorobenzene (132-3°) bromobenzene (155°) p cymene (176°) o-dichloro-benzene (180°) aniline (184°) methyl benzoate (200°) teti-alin (207°) ethyl benzoate (212°) 1 2 4-trichlorobenzene (213°) iaopropyl benzoate (218°) methyl salicylate (223°) n-propyl benzoate (231°) diethyleneglycol (244°) n-butyl benzoate (250°) diphenyl (255°) diphenyl ether (259°) dimethyl phth ate (282°) diethyl phthalate (296°) diphenylamine (302°) benzophenone (305)° benzyl benzoate (316°). [Pg.61]

The crystallized solid residue was washed with anhydrous ether to remove any unreacted benzoyl chloride. The 1-cyclohexylamino-2-propyl benzoate hydrochloride obtained was purified by two recrystallizations from absolute alcohol. It melted at 177° to 178.5°C. [Pg.768]

Benoit, F.M. Harrison, A.G. Hydrogen Migrations in Mass Spectrometry. II. Single and Double Hydrogen Migrations in the Electron Impact Fragmentation of Propyl Benzoate. Org. Mass Spectrom. 1976, 1056-1062. [Pg.324]

Propyl benzoate FALSE FALSE FALSE FALSE... [Pg.343]

See other pages where Propyl benzoates is mentioned: [Pg.544]    [Pg.544]    [Pg.780]    [Pg.782]    [Pg.782]    [Pg.787]    [Pg.787]    [Pg.419]    [Pg.461]    [Pg.485]    [Pg.607]    [Pg.1088]    [Pg.117]    [Pg.214]    [Pg.339]    [Pg.123]    [Pg.684]    [Pg.443]    [Pg.479]    [Pg.490]    [Pg.780]    [Pg.782]    [Pg.782]    [Pg.787]    [Pg.787]    [Pg.130]    [Pg.119]    [Pg.131]    [Pg.304]    [Pg.688]    [Pg.730]    [Pg.754]    [Pg.876]    [Pg.1357]    [Pg.268]    [Pg.307]    [Pg.329]    [Pg.780]    [Pg.782]    [Pg.782]    [Pg.787]   
See also in sourсe #XX -- [ Pg.443 ]

See also in sourсe #XX -- [ Pg.1078 ]



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N-Propyl benzoate

Propyl acetate benzoate

Propyl benzoate, hydrolysis

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