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3-Nitrobenzoyl nitrate

Acetyl nitrate, 0765 Benzoyl nitrate, 2689 Butyryl nitrate, 1573 3-Nitrobenzoyl nitrate, 2664... [Pg.29]

Nitrobenzoyl nitrate [101672-19-9] o U 0 0 o o YV o Francis, F. E., J. Chem. Soc., 1906, 89, 1 The nitrate explodes if heated rapidly, like benzoyl nitrate. See other ACYL NITRATES, NITROARYL COMPOUNDS c7h4n2o6... [Pg.940]

Acetyl nitrate, 0761 Benzoyl nitrate, 2685 Butyryl nitrate, 1568 3-Nitrobenzoyl nitrate, 2660... [Pg.2215]

Nitrobenzoyl peroxide,2 as well as w-nitrobenzoyl peroxide2 and anisoyl peroxide,3 have been prepared in about 50 per cent yields from the acid chlorides and an acetone solution of hydrogen peroxide, in the presence of a basic substance such as pyridine, sodium acetate, or sodium hydroxide. w-Nitrobenzoyl peroxide has also been prepared by nitration of benzoyl peroxide with cold... [Pg.33]

Di-(p-nitrobenzoyl)-furoxan5 Dll86 Dinitrobenzyl alcohol 2 B92 Dinitrobenzyl alcohol nitrate 3 B92 Dinitrobenzylamine 2 B93 Dinitrobenzylaniline 2 B93 Dinitrobenzylazide 2 B94—B95 Dinitrobenzyl benzoate 2 B9S Dinitrobenzyl cyanide 2 B96... [Pg.572]

If it is desired to obtain nitro-derivatives of 2-phenylbenzoselenazole in which the phenyl group in position 2 is nitrated, it is necessary that this nitro-group be present before condensation e.g. the zinc salt of o-aminophenyl selenide and p-nitrobenzoyl chloride when fused at 100° C. for an hour yield 2-(p-nitrophenvl)-benzoselenazole. [Pg.116]

In order to achieve the correct orientation in m-nitrobenzoyl chloride, oxidation of the methyl group must precede nitration. [Pg.561]

The reactions of the completely reduced compounds have attracted much attention because of their close relationship to piperazine. Thus it has been shown, as might be expected, that the 2-position in compounds such as the parent 100 can be readily acetylated and benzoylated" and ureas are formed with phenylisocyanate and phenylisothiocyanate." Compound 100 also reacts at the 2-position with p-acetamidobenzene-sulfonyl chloride to give a sulfonamide. There are several examples of the alkylation of the amine in the 2-position. Various alkyl halides -have been used, as well as ethylene oxide," p-nitrobenzoyl-ethyleneimine, " and l-guanyl-3,5-dimethylpyrazole nitrate. Compound 100 also undergoes the Eschweiler-Clarke modification of the Leuckart reaction to give the 2-methyl compound." ... [Pg.476]


See other pages where 3-Nitrobenzoyl nitrate is mentioned: [Pg.868]    [Pg.273]    [Pg.254]    [Pg.489]    [Pg.2116]    [Pg.2467]    [Pg.868]    [Pg.868]    [Pg.2034]    [Pg.2133]    [Pg.2377]    [Pg.100]    [Pg.101]    [Pg.241]    [Pg.868]    [Pg.273]    [Pg.254]    [Pg.489]    [Pg.2116]    [Pg.2467]    [Pg.868]    [Pg.100]    [Pg.101]    [Pg.267]    [Pg.868]    [Pg.2034]    [Pg.2133]    [Pg.2377]    [Pg.1006]    [Pg.199]    [Pg.403]    [Pg.2274]    [Pg.27]    [Pg.403]    [Pg.472]    [Pg.1006]    [Pg.1006]    [Pg.300]   
See also in sourсe #XX -- [ Pg.2 , Pg.90 ]




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