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Bis- 2,4-dinitro-phenyl

It was also prepd by heating bis(2,4-dinitro-phenyl)-sulfoxide with K2Cr207 in 57% sulfuric acid at its boiling temp (Refs)... [Pg.373]

C9. Capomacchia, A. C., Jennings, R. N., Hemingway, S. M., D Sousa, P., Prapaitrakul, W and Gingle, A., Native peroxyoxalate chemiluminescence from the reaction of bis (2,4-dinitro-phenyl) oxalate and hydrogen peroxide perturbed by non-fluorophores. Anal. Chim. Acta 196, 305-310 (1987). [Pg.164]

While the main field of application of chemiluminescence (CL) reactions is catalytic processes (e.g., oxidation of liuninol in the presence of metal ions), some noncatalytic reactions are also of great interest on accormt of the high sensitivity they provide. One of the most prominent of such reactions is that involving the hydrogen peroxide-induced oxidation of aryl oxalate esters in the presence of a suitable fluorescent species (Scheme 2). The most widely used aryl oxalates for this purpose are bis(2,4, 6-trichlorophenyl)oxalate (TCPO) and bis(2,4-dinitro-phenyl)oxalate. These CL reactions have been used... [Pg.2420]

Bis-[2.4-dinitro-phenyl]-ather des 4,5-DU DitTO-l.S-dioxy-anthinchmons 8, 461. [Pg.1582]

Bei der Umsetzung von 3,4-Bis-[cyclopropancarbonyl]-furazan-2-oxid mit 2,4-Dinitro-phenyl-hydrazin wird je nach Molverhaltnis neben einem Monohydrazon (Struktur unbekannt) ein Bis-hydrazon erhalten393 mit Phenylhydrazin tritt Ringspaltung ein (s. S. 754). [Pg.746]

CH3)2C6(N02)3] 2C(CH3)2 mw 522.43, N 16.09%, OB to C02 —107.2% yellowish crysts (from isoamyl ale), color deepens on exposure to light si sol in warm isoainyl ale decomposes with a slight explosion at 205°. Prepd by nitrating 2,2-Bis[2,4-dinitro-3,5-dimethyI-phenyl] propane with fuming sulfuric acid mixed with 97% nitric acid. Itisanexpl Refs 1) Beil 5, [527] 2) H. Goudet F. [Pg.78]

A closely related reaction is the conversion of 2,5-dimethylpyrrole into acetonylacetone bis-dinitrophenylhydrazone when it is boiled with 2,4-dinitro-phenyl hydrazine in 10 per cent sulphuric acid o, and certain reactions with hydrazine may be similar189, 323,... [Pg.88]

N. N -Dipicryl-ethylenedinitramine N,N -Bis(2,4,6 -trinitrophenyl-nitramino)- ethane N,N -Bis(2,4,6 -trinitrophenyl)- ethyl ene-dinitramine 2,4,6-T ri-nitro-1,3,5 tris(methylnitramino)- benzene 2,4,6,-2 , 4 6 -(B exanitrodiphenyD-ethylene-dinitramine Bitetryl or Ditetryl Its British name is Octyl [also called N,N>-Dinitro-N,N,-bis(2,4,6-trinitro-phenyl)-ethylenediamine Octanitroethylenedi-phenylamine and Bis-N(2, 4 ,6 -trinitropbenyl)... [Pg.131]

CijHjjNsOjS, rBenzol-5ulfons4ure-(l)]-<2 azo 4)-[l-(3- u]famoyl-phenyl)-pyrazolon-(5)-oarbaiis ure-[3)] 2S U 247, Ea8i nie-[bis-(2.6-dinitro-benz]rl)-amid] 181467. [Pg.1046]

The spectrophotometric method was calibrated with the l-fluoro,2,4-dinitro-benzene derivative of the model compound NN -bis(p-amino-phenyl) terephthalamide ... [Pg.26]

Inorganic analytical appHcations for ben2otrifluoride derivatives include sodiumtetrakis[3,5-bis(trifluoromethyl)phenyl]borate (Kobayashi s reagent) (345), and 4-(2,6-dinitro-4-trifluoromethylphenyl)aminoben2o-15-crown-5 (modified Takagi reagent (346). [Pg.333]

AI3-00040, see Cyclohexanol AI3-00041, see Cyclohexanone AI3-00045, see Diacetone alcohol AI3-00046, see Isophorone AI3-00050, see 1,4-Dichlorobenzene AI3-00052, see Trichloroethylene AI3-00053, see 1,2-Dichlorobenzene AI3-00054, see Acrylonitrile AI3-00072, see Hydroquinone AI3-00075, see p-Chloro-rrr-cresol AI3-00078, see 2,4-Dichlorophenol AI3-00085, see 1-Naphthylamine AI3-00100, see Nitroethane AI3-00105, see Anthracene AI3-00109, see 2-Nitropropane AI3-00111, see Nitromethane AI3-00118, see ferf-Butylbenzene AI3-00119, see Butylbenzene AI3-00121, see sec-Butylbenzene AI3-00124, see 4-Aminobiphenyl AI3-00128, see Acenaphthene AI3-00134, see Pentachlorophenol AI3-00137, see 2-Methylphenol AI3-00140, see Benzidine AI3-00142, see 2,4,6-Trichlorophenol AI3-00150, see 4-Methylphenol AI3-00154, see 4,6-Dinitro-o-cresol AI3-00262, see Dimethyl phthalate AI3-00278, see Naphthalene AI3-00283, see Di-rj-butyl phthalate AI3-00327, see Acetonitrile AI3-00329, see Diethyl phthalate AI3-00399, see Tributyl phosphate AI3-00404, see Ethyl acetate AI3-00405, see 1-Butanol AI3-00406, see Butyl acetate AI3-00407, see Ethyl formate AI3-00408, see Methyl formate AI3-00409, see Methanol AI3-00520, see Tri-ocresyl phosphate AI3-00576, see Isoamyl acetate AI3-00633, see Hexachloroethane AI3-00635, see 4-Nitrobiphenyl AI3-00698, see IV-Nitrosodiphenylamine AI3-00710, see p-Phenylenediamine AI3-00749, see Phenyl ether AI3-00790, see Phenanthrene AI3-00808, see Benzene AI3-00867, see Chrysene AI3-00987, see Thiram AI3-01021, see 4-Chlorophenyl phenyl ether AI3-01055, see 1.4-Dioxane AI3-01171, see Furfuryl alcohol AI3-01229, see 4-Methyl-2-pentanone AI3-01230, see 2-Heptanone AI3-01231, see Morpholine AI3-01236, see 2-Ethoxyethanol AI3-01238, see Acetone AI3-01239, see Nitrobenzene AI3-01240, see I idine AI3-01256, see Decahydronaphthalene AI3-01288, see ferf-Butyl alcohol AI3-01445, see Bis(2-chloroethoxy)methane AI3-01501, see 2,4-Toluene diisocyanate AI3-01506, see p,p -DDT AI3-01535, see 2,4-Dinitrophenol AI3-01537, see 2-Chloronaphthalene... [Pg.1457]

Its Lead Salt of 2,2 -bis(3,5-dinitro-4-hydroxy-phenyl>propane has been patented(Ref 4) as an ingredient, in admixture with KC103, or zirconium and NS, of ignition compositions and as being suitable for use in Electric Blasting Initiators... [Pg.147]

Sulfonyl-bis(2,6-dinitrophenol) in CA 5th Decennial Formula Index] [called Bis(3.5-dinitro -4-oxy-phenyl)-sulfon or 3.5.3 .5 -Tetranitro-4.4 -dioxy-diphenylsulfon in Ger], 0aS[(02N)2C6H2.0H]2 mw 430.27, N 13.02% very bitter-tasting straw-yel ndlsffrom boiling w), mp 257-258°(Ref 4) insol in most org solvs can be prepd by nitrating either bis(3-nitro-4-hydroxy-phenyl)-sulfone or bis(4-hydroxyphenyl)-sulfone and by hydrolyzing bis(3,5-dinitro-4-chlorophenyl) -sulfone(Refs 1 2). It forms salts which can be used in ignition compositions(Ref 3)... [Pg.148]

Hexonltro-3,3 -dimethyl-dlphenylamine or Bis(3-methyl-2,4,6-tri-nitro-phenyl)-amine, [CHJ.C4H(NOJ)3]2NH, bm tables (from ale), mp 60°. Can be prepd by warming 4,6-dinitro-3,3 -dimethyl-diphenyl amine with nitric acid(d 1.5) on a water bath. Its expl props were not investigated... [Pg.443]

Bis- 4-(dimethoxy-thiophosphorylthio)-3,5-dinitro-phenyl]- , /, 1-trichlor-ethan 75%... [Pg.716]

See other pages where Bis- 2,4-dinitro-phenyl is mentioned: [Pg.351]    [Pg.735]    [Pg.78]    [Pg.735]    [Pg.956]    [Pg.956]    [Pg.965]    [Pg.668]    [Pg.821]    [Pg.1196]    [Pg.351]    [Pg.735]    [Pg.78]    [Pg.735]    [Pg.956]    [Pg.956]    [Pg.965]    [Pg.668]    [Pg.821]    [Pg.1196]    [Pg.153]    [Pg.34]    [Pg.331]    [Pg.1139]    [Pg.308]    [Pg.412]    [Pg.412]    [Pg.326]    [Pg.428]    [Pg.315]    [Pg.51]    [Pg.158]    [Pg.27]    [Pg.186]    [Pg.702]    [Pg.779]    [Pg.585]    [Pg.956]    [Pg.964]   
See also in sourсe #XX -- [ Pg.689 ]



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