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4-ethoxyphenyl 2- 5-nitrophenyl

The reactions of 2-nitrophenyl benzyl tellurium4, 2-phenylazophenyl 4-ethoxyphenyl tellurium5, and l-oxo-l,3-dihydro-2-benzotellurophene6 with bromine that produce organo tellurium tribromides, very likely proceed via diorgano tellurium dibromides as intermediates. [Pg.319]

Dihydroxy-2-nitrophenyl)phenylmethanone, 624 [383382-96-5] [4-(Acetyloxy)-3-methoxy-2-nitrophenyl]phenylmethanone, 581 [383382-97-6] [4-(Acetyloxy)-3-methoxyphenyl]phenylmethanone, 582 [383382-98-7] (4-Hydroxy-3-methoxy-2-nitrophenyl)phenylmethanone, 581 [430459-44-2] Bis(5-fluoro-2,4-dihydroxyphenyl)metlianone, 642 [628263-26-3] (3,5-Dimethoxyphenyl)phenylmethanone, 566 [674786-33-5] (3-Ethoxyphenyl)(2,3,4-triliydroxyphenyl)methanone, 639 [680610-53-1] [2-Fluoro-3-(trifluoromethyl)phenyl](4-methoxyphenyl) methanone, 646... [Pg.2740]

Bromophenyl)-l-(4-methoxyphenyl)ethanone, 1704 2-Amino-l-(2,5-dimethoxyphenyl)ethanone (Hydrochloride), 1679 2-Bromo-l-(2-hydroxy-5-methyl-3-nitrophenyl)ethanone, 1655 l-(5-Chloro-2,4-dihydroxyphenyl)-2-(ethoxyphenyl)ethanone, 1708... [Pg.2834]

See other pages where 4-ethoxyphenyl 2- 5-nitrophenyl is mentioned: [Pg.431]    [Pg.249]    [Pg.431]    [Pg.5]    [Pg.41]    [Pg.79]    [Pg.297]    [Pg.241]   
See also in sourсe #XX -- [ Pg.552 ]

See also in sourсe #XX -- [ Pg.552 ]



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3- ethoxyphenyl

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