2- Chloro-3,5-dinitrobenzoic acid

Lopez, J.L., Einschlag, F.S.G., Rives, C.V., Villata, L.S., and Capparelli, A.L. Physiochemical and toxicological stndies on 4-chloro 3,5 dinitrobenzoic acid in aqneons solntions. Environ. Toxicol Chem., 23(5) 1129-1135, 2004. [Pg.1689]

Chloro 3.5 dinitrobenzoic acid benfluralin, trifluralin Chloroethanol oxadixyl, vamidothion... [Pg.1029]

Chlorobenzoic acid 4-Chloro-3,5-dinitrobenzoic acid 4-Chloro-3,5-dinitroaniline... [Pg.9]

Lopez JL, Garcia Einschlag FS, Gonzalez MC, Capparelli AL, Oliveros E, Hashem TM, Braun AM (2000) Hydroxyl Radical Initiated Photodegradation of 4-Chloro-3,5-dinitrobenzoic Acid in Aqueous Solution, J Photochem. Photobiol. A Chem. 137 177-184. [Pg.234]

EL Gross, A Curtiss, SR Durell and D White (1990) Chemical modification of spinach plastocyanin using 4-chloro-3,5-dinitrobenzoic acid Characterization of four singly-modified forms. Biochim Biophys Acta 1016 107-114... [Pg.633]

Keywords 4-chloro-3,5-dinitrobenzoic acid, 4-aminobenzoic acid... [Pg.418]

Chloro-3,5-dinitrobenzoic acid [118-97-8] M 246.6, m 159-161°, 163°, pKj st 2.5. Crystallise the acid from Et0H/H20, EtOH or The 1 1 naphthalene complex (by fusing various ratios of ingredients and... [Pg.298]

The halogen in an aromatic compound (e.g., 4-chloro-3,5-dinitrobenzoic acid) can be made to react with amino group (e.g., p-aminobenzoic acid) in solid state at 180° C to give the corresponding amine (Scheme 21). [Pg.200]

SM) in refluxingethanol for 20 min (75%). SM was prepared from p-chlorobenzoic acid by a three-step synthesis at first, nitration of this acid with nitric add/con-centrated sulfuric acid at 140° for 1.5 h. The 4-chloro-3,5-dinitrobenzoic acid formed (95%, m.p. 159°), on treatment with phosphorous pentachloride in refluxing benzene gave the 4-chloro-3,5-dinitrobenzoyl chloride. Then, by adding aluminium chloride to the reaction mixture and heating this one in a water bath for 30 min, SM was obtained (90%, m.p. 118°) [496]. m.p. 138° [140], 136° [496] Spectra (NA). [Pg.50]

The effects of CDNB (4-chloro-3,5-dinitrobenzoic acid) modification at lysines 1, 54, 71, and 77 in spinach plastocyanin on the kinetics of electron transfer with [Fe(CN)e] , cytochrome c(III), and cytochrome /(III) have been examined. The modifications have little effect on the rate constants for oxidation by the ferricyanide, while rate enhancements and inhibitions (except for lysine 71) are observed for the reactions with cytochrome c and cytochrome / respectively. [Pg.29]

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