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O-Cresyl benzoate

Cinnamon (Cinnamomum zeylanicum) bark oil Cinnamyl benzoate Cinnamyl cinnamate Cinnamyl formate Cinnamyl isovalerate Cinnamyl phenylacetate Cinnamyl propionate Citral diethyl acetal Citronellyl phenylacetate Clove (Eugenia caryophyllusj extract Cod liver oil Coffee (Coffea arabica) bean extract m-Cresol o-Cresol p-Cresol o-Cresyl acetate p-Cresyl acetate Cuminic alcohol Cumin (Cuminum cyminum) oil Cyclohexanol... [Pg.5025]

Amino-6-ethoxybenzothiazole C9HioN402S2 Sulfamethizole C9H10O 2-Ally I phenol Cinnamyl alcohol 2,4-Di methyl benzal dehyde p-Ethylbenzaldehyde Ethyl phenyl ketone Hydrocinnamaldehyde 4 -Methyl acetophenone 2-Phenyl propanal Propiophenone p-Tolylacetaldehyde C9H10O2 Acetanisole Benzyl acetate m-Cresyl acetate o-Cresyl acetate p-Cresyl acetate p-Ethoxybenzaldehyde Ethyl benzoate Hydrocinnamic acid 2-M ethoxy-4-vi nyl phenol a-Methylbenzyl formate Methyl phenylacetate Methyl p-toluate Phenethyl formate Phenyl glycidyl ether... [Pg.7060]

Preparation by Fries rearrangement of m-cresyl. =./ / o-chloro-benzoate,... [Pg.235]

Preparation by Fries rearrangement of p-cresyl o-chloro-benzoate in the presence of aluminium chloride [23] without solvent at 120° and 160° [132,919,920], (71%) [1087]. [Pg.235]

Preparation by Fries rearrangement of o-cresyl p-chloro-benzoate with aluminium chloride without solvent at 120°and 160° (good yield) [926], (52%) [1087]. [Pg.240]

Obtained by Fries rearrangement of o-cresyl / m-methoxy-benzoate with aluminium chloride... [Pg.431]

See other pages where O-Cresyl benzoate is mentioned: [Pg.789]    [Pg.789]    [Pg.789]    [Pg.1360]    [Pg.1360]    [Pg.789]    [Pg.789]    [Pg.271]    [Pg.223]    [Pg.179]    [Pg.789]    [Pg.789]    [Pg.789]    [Pg.1360]    [Pg.1360]    [Pg.789]    [Pg.789]    [Pg.271]    [Pg.223]    [Pg.179]    [Pg.78]    [Pg.75]    [Pg.1595]    [Pg.63]    [Pg.34]    [Pg.77]    [Pg.82]    [Pg.34]    [Pg.4458]    [Pg.5548]    [Pg.236]    [Pg.248]   
See also in sourсe #XX -- [ Pg.271 , Pg.350 ]



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2-[O-Cresyl

O-Cresylic

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