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・ 3-D Ultra Pinball
・ 3-Deazaneplanocin A
・ 3-dehydro-L-gulonate 2-dehydrogenase
・ 3-dehydro-L-gulonate-6-phosphate decarboxylase
・ 3-Dehydrocarnitine
・ 3-dehydroquinate dehydratase
・ 3-dehydroquinate synthase
・ 3-dehydroquinate synthase II
・ 3-Dehydroquinic acid
・ 3-dehydroshikimate dehydratase
・ 3-Dehydroshikimic acid
・ 3-dehydrosphinganine reductase
・ 3,3',5,5'-Tetramethylbenzidine
・ 3,3',5-Triiodothyronamine
・ 3,3'-Diaminobenzidine
3,3'-Dichlorobenzidine
・ 3,3'-Diindolylmethane
・ 3,3'-Diiodothyronine
・ 3,3,4,4-Tetramethyltetrahydrofuran
・ 3,3,4,4-Tetramethyltetrahydrofuran-2,5-dione
・ 3,3-Bis(chloromethyl)oxetane
・ 3,3-Diethyl-2-pyrrolidinone
・ 3,3-Diphenylcyclobutanamine
・ 3,3-Diphenylpropylamine
・ 3,4,5-Tri-O-galloylquinic acid
・ 3,4,5-Trimethoxybenzaldehyde
・ 3,4,8-Trimethoxyphenanthrene-2,5-diol
・ 3,4-Dehydroadipyl-CoA semialdehyde dehydrogenase (NADP+)
・ 3,4-Diaminopyridine
・ 3,4-Dichloroamphetamine


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3,3'-Dichlorobenzidine : ウィキペディア英語版
3,3'-Dichlorobenzidine

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3,3'-Dichlorobenzidine is an organic compound with the formula (C6H3Cl(NH2))2. The pure compound is pale yellow, but commercial samples are often colored. It is barely soluble in water and is often supplied as a wet paste. It is widely used in the production of diarylide dyes and diarylide yellow pigments used in the production of printing inks.〔K. Hunger. W. Herbst "Pigments, Organic" in ''Ullmann's Encyclopedia of Industrial Chemistry'', Wiley-VCH, Weinheim, 2012. 〕
==Preparation and reactions==
3,3'-Dichlorobenzidine is prepared in two steps from 2-nitrochlorobenzene. The first step involves reduction with zinc in base to afford 3,3'-dichlorodiphenylhydrazine. This intermediate undergoes the benzidine rearrangement to afford 3,3'-dichlorobenzidine.
Aqueous solutions of 3,3'-dichlorobenzidine degrade in light to monochloro derivative. It undergoes chlorination (for example in water treatment plants) to give the tetrachloro derivative.
The most widely practiced reaction of 3,3'-dichlorobenzidine is its double diazotization to afford ()2+. This intermediate is then coupled to derivatives of acetoacetylaminobenzene (CH3C(O)CH2C(O)NHAr).〔

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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