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2,6-Dinitro-2 -hydroxy

Bis[Dinitro-hydroxy-azo-quinone], called by v. Herz sym-Tetranitro-dioxy-diphenol-quinone-tetrazide, or Tetranitro-diresorcin-diazo-anhydride... [Pg.72]

Dinitroanilinoyethanol N-(2,4-Dinitrofphenylethanolamine 2,4 Dinifro-phenylaminoethanol 2-4 Dinitro-hydroxy-ethylaniline or 2,4-Dinitro-l-( -hydroxy-ethyl)-aminobenzene (OjN)j CjHj-NH-CHj -CH,-OH, mw 227.18, N 18.50%. Orange-yel crysts, mp 89-92°. Was prepd by Moran (Ref 2) from 2,4-dinitroch loro benzene and aminoethanol. This method is described by Clark(Ref 3). Other methods of prepn are described in Refs 4 5. On nitration this compd yields the hi ly explosive 2-(2, 4, 6 trinitro-N-nitranilino)-ethanol nitrate, designated as Pentryl(See p A425)... [Pg.424]

Naphthalenol also is used ia the preparation of azo, iadigoid, and nitro, eg, 2,4-dinitro-l-naphthol, dyes, and ia making dye iatermediates, eg, naphtholsulfonic acids, 4-chloro-1-naphthalenol, and l-hydroxy-2-naphthoic acid. 1-Naphthalenol is an antioxidant for gasoline, and some of its alkylated derivatives are stabilizers for plastics and mbber (68). [Pg.498]

Following the 3,4-dihydroisoquinolinium compounds, the isoquino-linium compounds themselves will now be considered. The violet red compound obtained by Zincke by heating i-hydroxy-2-(2,4-dinitro-phenyl)-l,2-dihydroisoquinoline (16a) is the open-chain amino-aldehyde (17) isomeric with (16a) and is not the hemiacetal (18) as assumed by Zincke. This is the first case in which both the members... [Pg.179]

Methyl-[ 5,7-dinitro-8-hydroxy-naphthyl-(l)] -ether, 2,4-Dinitro-8-methoxy-naphthol-(l) ). (02N)2CioH4(OH).O.CH3, mw 264.21, N 10.61%, OB to C02 -121.12%, gold plates from ale, mp 179—80° (decompn). Sol in dil alkali ale. Prepn from 2,4-dinitro-1,8-dime thoxy-naphthalene by reaction with 2N NaOH Ref Beil 6, 5284 ... [Pg.111]

Di n itr o-8- Hyd roxy 1 -Acetoxy-Naphtha bob (2,4-Dinitro-8-acetoxy-naphthol-(l), acetic acid-r >.7-dinit.ro-8-hvdrnxv-nanhthv14r1 V tf rl f5 7. dinitro-8-hydroxy-naphthyl-(l)-acetate]. H0.(O2N)2C10H4.OCOCH3, mw 292.22, N 9.59%, OB to C02 —149.81%, gold prisms from AcOH, mp 200° (decompn). Sol in ale boiling AcOH. Prepn from 1,8-diacetoxy-naphthalene by reaction with dil nitric acid (d 1.4g/cc) at 25-30°... [Pg.202]

Trinitro-1-Naphthol (2,4,5-Trinitro-1-hydroxy naphthalene). Yellow leaflets or prisms mp 189—90° bp, explds. Sol in hot AcOH, si sol in hot w, ale, benz, eth acetate, xylene cold AcOH. Prepn from 2,4-dinitro-naphthol by nitration, or from 4-chlor-1,3,8-trinitronaphthalene by heating with 0.1 N NaOH in w or ale... [Pg.202]

The Postnitrated Polyurethane Polymer of 3,6-Dinitro-3,6-Diaza-1,8-Octane Diisocyanate with N,N -Bis (2-Hydroxy ethyl) Oxamide. [Pg.339]

Acetyl-phenyl- 635 4-Amino-3,5-dimethyl-phenyl- 102 2-Amino-4-hydroxy-phenyl- 692 4-Amino-phenyl- 685 4-Benzylamino-phenyl- 102 2,4-Dinitro-phenyl- 692 4-(2-Hydroxy-benzylamino)-phenyl- 102 2-(2-Methyl-butanoyl)-phenyl- 635 4-Methoxy-2,6-dimethyl-phenyl-102 (Nitro-phenyl)- 635 2-Nitro-phenyl- 680, 692 4-Nitro-phenyl- 685... [Pg.923]

Dimethylamino-methyl)-2-hydroxymethyl-aus 2 -Carboxy-2-(dimethylaminocarbonyl)-biphenyl und Lithiumalanat 165 2,2 -Dinitro- 474, 476, 695 6,6 -Dinitro-2,2 -bis-[chlorcarbonyl]- 188 2,2 -Dinitro-4,4 -bis-[diathylamino]- 695 4,4 -Dinitro-2,2 -bis-rhydroxymethyl]- 213 6,6 -Dinitro-2,2 -bis-[hydroxymethyl]- 188 2,2 -Dinitro-4,4 -diamino- 695 6,6 -Dinitro-2,2 -diformyl- 694 4,4 -Dinitro-2,2 -dimethoxycarbonyl- 213 2,2 -Dinitro-4,4 -dimethyl- 695 6,6 -Dinitro-2 -formyl-2-carboxy- 694 2,2 -Dinitroso- 476 -4-hydroxamsaure-chlorid 537 4-(a-Hydroxy-benzyl)- 542 Methoxy- 678 2-Methyl- 556 Nitro- 672, 678 4-Nitro- 687... [Pg.976]

Another host, 2-hydroxy-3,5-dinitro-N -(5-nitrofurfurylidene)benzohydrazide (6),... [Pg.17]

Other common intermediates for azo pigment production are 2,4-dinitro-aniline, acetoacet-o-chloroanilide, acetoacet-o-toluidide, phenyl- and p-tolyl-methylpyrazolone, 2-hydroxy-3-naphthoic acid, Naphtol AS and its derivatives, and 2-chloro-4-aminotoluene-5-sulfonic acid. [Pg.193]

Diethyl (V-(2-hydroxyphenyl)aminomethylenemalonate was reacted with 2,4-dinitro-l-chlorobenzene in boiling aqueous ethanol in the presence of sodium hydrogen carbonate for 4 hr. After work-up, 2-hydroxy-2, 4 -dinitrodiphenylamine, obtained in 76% yield, failed to react with EMME under the usual conditions (89CCC506). [Pg.308]

Ethyl-4-hydroxy-l,2,5-oxadiazole, 1504 4-Oximino-4,5,6,7-tetrahydrobenzofurazan A-oxide, 2357 Potassium 4-hydroxyamino-5,7-dinitro-4,5-dihydrobenzofurazanide 3-oxide, 2176... [Pg.165]


See other pages where 2,6-Dinitro-2 -hydroxy is mentioned: [Pg.201]    [Pg.350]    [Pg.696]    [Pg.202]    [Pg.72]    [Pg.424]    [Pg.424]    [Pg.72]    [Pg.1016]    [Pg.892]    [Pg.295]    [Pg.105]    [Pg.209]    [Pg.111]    [Pg.111]    [Pg.201]    [Pg.202]    [Pg.202]    [Pg.12]    [Pg.555]    [Pg.891]    [Pg.59]    [Pg.91]    [Pg.685]    [Pg.390]    [Pg.533]    [Pg.238]    [Pg.3]    [Pg.80]    [Pg.962]    [Pg.506]    [Pg.825]    [Pg.1491]   
See also in sourсe #XX -- [ Pg.350 , Pg.351 ]




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