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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