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4,6-Dinitro-l-

Chloro-1,3-dinitro-5-trilluoromethylbenzene, 2637 Dimethyl 4-acetamidophthalate Nitric acid, 3520 4,6-Dinitro-l,3-benzenediol, 2198 Dinitrogen tetraoxide, Laboratory grease, 4747... [Pg.266]

Dinitro-l, 3-diaminobenzene, yel prisms (from AcOH) si sol in ale somewhat more sol in glac AcOH (Ref 3) ... [Pg.24]

Dinitro-l, 3-bis( f -hy droxyetby lamino)-benzene orn-yel ndls (from ale), having a bitter taste, mp 211° practically insol in eth, petr eth, chlf, benz Sc toluene si sol in w, was prepd by treating an alcoholic soln of 1,3-dichloro-4,6-dinitrobenzene with 4 equivs of jS-hydroxyethylamine (Ref 3). [Pg.136]

Dinitro-l,3-difluorohenzene (DNDFB) or 2,4-Dinitro-l-difluorobenzene (DNFFB) (called 4.6-Difluor-1.3-dinitro-benzol in Ger), prisms (from ale), mp 73-75° readily sol in hot ale less sol in cold ale can be prepd by nitrating either 1,3-difluorobenzene or 1-nitr o-2,4-di fluoro benzene with mixed acids (Ref 1) or by other methods (See Refs)... [Pg.153]

Dinitro-l,3-dihydroxybenzene, or 4,6-Dinitroresorcin (4,6-DNR), yel prisms (from eth acetate), mp 212-15°. Was first prepd in... [Pg.169]

Trinitro-N,N-dimethylaniline, om-red crysts (from acet or benz), mp 198°, sp gr 1.585 at 17° Can he prepd by heating N,N-di-methyl-N -phenyl-4,6-dinitro-l, 3-phenylene-diamine with aniline ale in a tube at 110—20°, or by other methods (Ref 10)... [Pg.209]

Dinitro-l, 3-dime tbylbenzene, col prisms (from ale), mp 92—94°, bp—explodes prepd by nitrating m-xylene with coned nitric acid at RT (Ref 1, P380 Ref 2, pl84 Ref 3, p295 Ref 4, p844)... [Pg.217]

Diplumbic Dinitroresorcinol. See Basic Lead Salt of 4,6-Dinitro-l, 3-dihydroxy benzene or Lead 4,61 Din itro resorcin ate, p D1275-.R... [Pg.384]

Dinitro-2-chloro-N-methylaniline, yel nds (from ale), mp 133° was prepd by reaction of 4, 6-dinitro-l,2-dichlorobenzene with an ale soln of methylamine(Ref 6)... [Pg.43]

Base-catalyzed condensation (Equation 31) of 4,6-dinitro-l-tosylindoline with salicylaldehyde or 2-hydroxy-naphthalene-l-carbaldehyde is accompanied by intramolecular nucleophilic substitution for one of the nitro groups to give benzo- and naphthooxepino[4,3,2-crf indoles, respectively <2003IZV725>. [Pg.65]

See other pages where 4,6-Dinitro-l- is mentioned: [Pg.716]    [Pg.1082]    [Pg.1131]    [Pg.1579]    [Pg.330]    [Pg.335]    [Pg.235]    [Pg.628]    [Pg.136]    [Pg.225]    [Pg.281]    [Pg.289]    [Pg.479]    [Pg.488]    [Pg.559]    [Pg.563]    [Pg.572]    [Pg.574]    [Pg.574]    [Pg.574]    [Pg.578]    [Pg.45]    [Pg.50]    [Pg.156]    [Pg.368]    [Pg.618]    [Pg.797]    [Pg.1139]    [Pg.1186]    [Pg.1645]    [Pg.2393]    [Pg.2543]   
See also in sourсe #XX -- [ Pg.349 ]



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1- Methyl-3,5-dinitro-l,4-dihydropyridin-4one, conversion to furo pyridine

1.2- Dinitro-l,2-ethylene derivs

2,4-Dinitro-l-naphthol

2- Chloro-3,6-dinitro-l ,8-naphthyridine

2.2- dinitro-l ,3-propanediol

2.4- Dinitro-l-fluor

2.4- Dinitro-l-methoxy

2.4- Dinitro-l-methyl

2.4- Dinitro-l-naphthylamine

3.5- Dinitro-l,2,4-triazole, reaction with oxiranes

3.5- dinitro-l,2,4-triazole

Benzene, l-Chloro-2,4-dinitro

Sodium polysulfide as agent to reduce l,3-dinitro-4,6-diaminobenzene

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