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Dinitro compds

By addition of nitrogen dioxide, nitrosates (II) (nitroso-nitrates) or dinitro compds (III) or dinitrites (IV) are obtained. Nitrosates (II) can be oxidized to nitro-nitrates (Ila), viz ... [Pg.422]

Schaarschmidt and Hoffrneier (Ref 2) found that on treating an unsaturated hydrocarbon with NLQ4 a mixt of products of the I, II III and IV types was obtained. Only the dinitro compds of type III were stable. Others underwent decomposition in the following way ... [Pg.422]

Bachmann et al (Ref 17) investigated possibilities of prepn of EDNA from the following dinitro compds l,3-Dinitro 2-imidazolidone Dinitroethylenebisurethane NtN -Diniwoethylene-bisacetamide N.N -Dmitroethyleneoxamide and 3,3/"Dinitro-l,l/-ethylenebisurea, and he found that EDNA could be obtd from any of these compds with the exception of the 3,3,-Di nitro-1,1 -ethylenebisurea... [Pg.112]

Felhoen Powder — patented in England in 1879 consisted of 90p of Black Powder with 10p of a product obtained on nitration of naphthalene (lp) with 4parts of nitric acid (d 1,4). The nitrated product consisted of mononitronaphthalene with a small amount of the dinitro-compd Ref Daniel (1902), 298... [Pg.395]

N 24.38%. The following derivs are the more important dinitro compds ... [Pg.51]

On nitration it gives an expl dinitro compd and also forms salts, some of which are expl, as for example ... [Pg.193]

Dinitro compd is an expl comparable in sensitivity to impact to TNT it is very hygroscopic and hydrolizable by hot w does not possess good thermaL stability (decomposes... [Pg.229]

N.N -Dinilro-N.N -dietbyl-sulfamide (See under Dinitro compds in this Vol)... [Pg.267]

Blanksma Fohr (Ref 2) reported. prepn of the 2,4,6-trinitro deriv, mp 104°, bitter taste, by nitrating the dinitro compd with anhyd nitric acid sulfuric acid at 0°for... [Pg.286]

Dinitroabietic Acids. The dinitro compd of the formula (OaN)a C19Ha7.COOH, mp 178— 184°, reported to be obtained by Johansson on nitrating abietic acid (Refs 1 2),could not be identified as dinitroabietic acid by later investigators. Goldblatt et al(Refs 3 ... [Pg.3]

Note M.Berthelot, CR 65,508(1867), tried to obtain an explosive by nitration of acenaph-thene but the highest product of nitration was a non-explosive dinitro compd which melted with decompn at 206°. The same product was later prepd by F.Sachs and G.Mosenbach,... [Pg.12]

Another dinitro-compd, called by Fran-chimont Klobbie isodinitroglycolurlle f wh microscop crysts,insol in ordinary org solvents and sol in coned nitric acid was also obtained from acetylenediurein and absol nitric acid. It was distinguished from the first isomer by the fact that the latter was not decomp on heating with w but was decompd by aq ammonia at RT (Refs 1 3) Refs l)BeiI 26, 443 2)A.Franchimont... [Pg.66]

Aminopseudocumenes or Amino-l,2,4-trimethyl benzenes,(CH,)sC6H2 NH2. Several isomers are known of vfiich the 5-ctminopseudocianene is the most important. Its mono- and dinitro- compds are known but they are not expl. Azido- and diazido- derivs were not found in Beil or CA through 1956... [Pg.254]

N 23.33% It yel cryst pdr, mp dec with evoln of gas expl when heated suddenly was prepd by treating the above bis(dinitro-dinitro-) compd, C3qH2sN1 2Ot6, with abs nitric acid, cooled to -15 (Ref 2,p 415-16)... [Pg.154]

The dinitro compd forms expl salts such as the Mercurous Salt, C2N504Hjg mw 363.66 ... [Pg.858]

Nearly all metallic salts of the dinitro compd, especially those of Pb, Ba Ag are explosive(Refs 1 3)... [Pg.420]

Di jiifro-2f2 osoRophthole ns (c ailed 2,2 -azobis [4-nitronaphthalene in CA) brn-red crysts, mp 315°. Prepd from the action of hydrazine in ale on l-chloro-2,4-dinitro-naphthalene, warmed 6 hrs on a w bath. The product was a mixt of the dinitro compd, the di-NH4 salt of 2,4-C10H6(NO2)2, m-nitro-naphthylazimidole and some 2,4-dimtro naphthalene. The reaction of anhyd hydrazine with l-chIoro-2.4-dinitronaphthalene gave only the 4,4 -dinitro-2,2 -azonaphthaiene and 2,4-dinitronaphthalene (Refs 1 2)... [Pg.656]

When treated with weak nitric acid it rendered the dinitrate, while strong nitric acid gave the dinitro compd... [Pg.106]

Dinitro-2,2 -diet boxy azobenzene brownishared ndls (from chlf) mp 284-5° sublimes without decompn sol in cold chlf or cold benz insol in boiling ale dissolves without decompn with a yel-red color in cold coned H2SO4. It was obtd together with the z,z -dinitro compd on nitrating 0,0 -azophenetol... [Pg.657]


See other pages where Dinitro compds is mentioned: [Pg.760]    [Pg.33]    [Pg.237]    [Pg.262]    [Pg.656]    [Pg.657]    [Pg.67]    [Pg.84]    [Pg.110]    [Pg.113]    [Pg.374]    [Pg.54]    [Pg.740]    [Pg.657]    [Pg.53]    [Pg.703]    [Pg.254]   


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