翻訳と辞書 ・ 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
|Section2= |Section3= }} 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)』 ■ウィキペディアで「3,4-Xylidine」の詳細全文を読む
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