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Bibenzyl 4,4 -dinitro

N 18-58%, OB to C02 -70.8%. Pale yel crysts, mp 213-218°. Will(Ref 2) claimed that he prepd the compd with mp 212° either by nitration of dinitro-bibenzyl or by oxidation of a-TNT, but he gave no detailed procedures. Rinkenbach Aaronson(Ref 3) obtained it in a very small quantity [together with a large amt of 2,4,2 ,4 ,6 -pentanitro-a-hydrox-ybibenzil, (02N)3CeH,.CH2.CH(0H).C6H3(N02), also called a-2,4,6-trinitrophenyl-jS-2,4-dinitro-phenyl-hydroxyethane] when they nitrated the previously sulfonated tetranitrobibenzyl by a rather complicated procedure. Mecir(Ref 3a) claimed to have prepd the hexanitro-compd by treating a-TNT with an aq soln of Na sulfite... [Pg.111]

See other pages where Bibenzyl 4,4 -dinitro is mentioned: [Pg.45]    [Pg.35]    [Pg.86]    [Pg.81]    [Pg.95]    [Pg.52]    [Pg.44]    [Pg.54]    [Pg.45]    [Pg.35]    [Pg.86]    [Pg.110]    [Pg.127]    [Pg.81]    [Pg.95]    [Pg.52]    [Pg.44]    [Pg.54]   
See also in sourсe #XX -- [ Pg.34 , Pg.35 ]

See also in sourсe #XX -- [ Pg.5 , Pg.34 ]

See also in sourсe #XX -- [ Pg.34 , Pg.35 ]

See also in sourсe #XX -- [ Pg.34 , Pg.35 ]



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