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Dibromo-acetamide

Beilstein Handbook Reference) Acetamide, 2-cyano-2,2-dibromo- Acetamide, 2,2-dibromo-2-cyano- Amerstat 300 Biosperse 240 BRN 1761192 Caswell No. 287AA Dbnpa ... [Pg.190]

Chemical Name Acetamide, N-(2,4-dibromo-6-((methyltricyclo [3.3.1.13,7]dec-l-ylamino)methyl)phenyl)-... [Pg.97]

V. Braun reaction Cyanogen bromide. Phosphorus tribromide. Piperidine. Thionyl chloride. Bromination Aluminum bromide. Aluminum chloride. Boron tribromide. Bromine chloride. N-Bromocaprolactam. N-Bromosuccinimide. Bromotrichloromethane. Cupric bromide. Dibenzoyl peroxide. l,3-Dibromo-5,5-diraethylhydantoin. 1,2-Dibromotetrachloromethane. HBr-scavengers acetamide and potassium chlorate. Iodine. Iodine monobromide. Iron. Mercuric acetate. Phenyl trimethylammonium perbromide. Phosphorus trichloride. Pyridine. Pyridine perbromide. Pyridinium hydrobromide perbromide. Silver sulfate. Sodium acetate. Sodium hypobromite. Sulfur. Sulfur monochloride. Tetramethylaramonium tribromide. M-Tribromoacetophenone. Trichloromethane sulfonyl bromide. Trilluoroacetyl hypobromite. Triphenylphosphine dibromide. [Pg.655]

Acetamide, 2-(2-benzothiazolyloxy)-N-methyl-N-phenyl-. SeeMefenacet Acetamide, 2-chloro-. See Chloroacetamide Acetamide, 2,2-dibromo-2-cyano-. See 2,2-Dibromo-3-nitrilopropionamide Acetamide, N,N -1,2-ethanediylbis-n-acetyl-. [Pg.29]

It may be possible that in some production regimes new concepts of combining a slow acting but stable active ingredient for in-can preservation with a very fast but unstable sacrifice microbicide like 2,2-dibromo-2-cyano-acetamide (DBNPA) [II, 17.5.] to eradicate existing microbial burden from raw materials will gain importance. [Pg.358]

The deprotonation of BSA using lithium diisopropylamide was used to generate the protected acetamide enolate ion for use in the synthesis of the dienone shown in eq 22. It has been shown subsequently that the same product can be prepared by the reaction of the anion, generated from n-butyllithium and BSA, with 2,6-dibromo-l,4-benzoqurnone. The anion has also been used in reactions with a number of carbonyl compounds, including benzophenone. ... [Pg.62]

The first two members of this series, 2,6-dibromo-4-acetamide-4-hydroxycyclo-hexadienone (1) and the dimethoxyketal 2, were isolated from the methanolic extracts of Verongia fistularis and V. cauliformis by Shanna and Burkholder in 1967 (2-4). Anderson and Faulkner isolated a mixed methoxy-ethoxy ketal 3 from Verongia sp. in 1973. Since the H NMR spectrum of 3 showed two methoxy signals, indicating that 3 is a mixture of two diastereoisomers, 2 and 3 were considered as artifacts generated during the extraction process (5). Faulkner et al. also reported the dienone 4 from Tylodina fungina (6). [Pg.61]


See other pages where Dibromo-acetamide is mentioned: [Pg.274]    [Pg.274]    [Pg.50]    [Pg.54]    [Pg.54]    [Pg.59]    [Pg.48]    [Pg.220]    [Pg.385]    [Pg.51]    [Pg.255]    [Pg.576]    [Pg.274]    [Pg.350]    [Pg.59]    [Pg.58]   
See also in sourсe #XX -- [ Pg.274 ]




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