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Acetamidobenzene

Acetamidobenzene—3—diazoniumhydraxide or l-Acetamino-3-diazonium hydroxide-benzene (N-Acetyl-3-diazoniumhydroxide-aniline Acetanilide-3-diazoniumhydroxide),... [Pg.18]

Acetamidobenzenesulfonyl azide is obtained from Aldrich Chemical Company, Inc., and used without further purification. In addition, 4-acetamido-benzenesulfonyl azide can be synthesized from the precursor, 4-acetamidobenzene-sulfonyl chloride.2... [Pg.231]

ACETAMIDE, N-PHENYL- see AAQ500 5-ACETAMIDE-l,3,4-THI.ADIAZOLE-2-SULFONAMIDE see. AAI250 ACETAMIDOBENZENE see. AAQ500... [Pg.1488]

ACETAMIDOBENZENE (103-84-4) A combustible solid (flash point 345°F/174°C). Reacts with strong oxidizers and strong bases. UV light can cause chemical alteration (the acetyl group forms a new bond on ring in the o- or p-position). [Pg.3]

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 Acetamidobenzene is mentioned: [Pg.1005]    [Pg.1005]    [Pg.1006]    [Pg.1007]    [Pg.98]    [Pg.430]    [Pg.1609]    [Pg.1925]    [Pg.1232]    [Pg.1232]    [Pg.1233]    [Pg.76]    [Pg.313]    [Pg.18]    [Pg.18]    [Pg.1005]    [Pg.1006]    [Pg.450]    [Pg.18]    [Pg.18]    [Pg.82]    [Pg.884]    [Pg.286]    [Pg.291]    [Pg.1195]    [Pg.1917]    [Pg.1920]    [Pg.1923]    [Pg.884]    [Pg.16]    [Pg.18]    [Pg.18]    [Pg.18]    [Pg.18]    [Pg.22]    [Pg.735]    [Pg.1005]    [Pg.1005]    [Pg.1006]    [Pg.9]    [Pg.3]    [Pg.1005]    [Pg.1005]    [Pg.1006]   
See also in sourсe #XX -- [ Pg.670 , Pg.671 ]




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P-Acetamidobenzene sulfonyl

P-Acetamidobenzene sulfonyl chloride

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