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・ 3,4-Dimethoxyphenethylamine
・ 3,4-Dimethoxystyrene
・ 3,4-Dimethylmethcathinone
・ 3,4-Divanillyltetrahydrofuran
・ 3,4-Epoxycyclohexanecarboxylate methyl ester
・ 3,4-Epoxycyclohexylmethyl-3’,4’-epoxycyclohexane carboxylate
・ 3,4-Ethylidenedioxyamphetamine
・ 3,4-Methylenedioxy-N-hydroxy-N-methylamphetamine
・ 3,4-Methylenedioxy-N-isopropylamphetamine
・ 3,4-Methylenedioxy-N-methoxyamphetamine
・ 3,4-Methylenedioxy-N-methylphentermine
・ 3,4-Methylenedioxy-N-propylamphetamine
・ 3,4-Methylenedioxyphenylpropan-2-one
・ 3,4-Methylenedioxypropiophenone
・ 3,4-Xylenol
3,4-Xylidine
・ 3,4′-Dihydroxystilbene
・ 3,5,7-Trioxododecanoyl-CoA synthase
・ 3,5-Di-tert-butylsalicylaldehyde
・ 3,5-Dihydroxy-4-isopropyl-trans-stilbene
・ 3,5-Dihydroxybenzoic acid
・ 3,5-Dihydroxycinnamic acid
・ 3,5-Dihydroxyphenylpropionoic acid
・ 3,5-Diiodothyronine
・ 3,5-Dimethylpiperidine
・ 3,5-Dinitrobenzoic acid
・ 3,5-Dinitrosalicylic acid
・ 3,7-dimethylquercetin 4'-O-methyltransferase
・ 3,7cm KPÚV vz. 34
・ 3,7cm KPÚV vz. 37


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3,4-Xylidine : ウィキペディア英語版
3,4-Xylidine

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3,4-Xylidine (3,4-dimethylaniline) is a organic compound with formula (CH3)2C6H3NH2. It is an aromatic amine and a xylidine isomer. It is a crystalline solid.〔M. Meyer "Xylidines" in ''Ullmann's Encylclopedia of Industrial Chemistry'', Wiley-VCH, Weinheim, 2012. 〕
==Preparation and applications==
The compound is prepared by two routes: hydrogenation of (2-chloromethyl)-4-nitrotoluene and reaction of the bromoxylene with ammonia. It is a precursor for the production of riboflavin (vitamin B2).〔

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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