翻訳と辞書 ・ N'Zoo ・ N'Zébéla ・ N'écoutez pas ・ N(6)-Carboxymethyllysine ・ N+ ・ N++ ・ N+1 ・ N+1 redundancy ・ N,alpha-Diethylphenylethylamine ・ N,N'-Di-2-butyl-1,4-phenylenediamine ・ N,N'-Di-n-butylthiourea ・ N,N'-diacetylbacillosaminyl-diphospho-undecaprenol alpha-1,3-N-acetylgalactosaminyltransferase ・ N,N'-diacetylchitobiose phosphorylase ・ N,N'-diacetyllegionaminate synthase ・ N,N'-Dicyclohexylcarbodiimide ・ N,N'-Diisopropylcarbodiimide ・ N,N'-Methylenebisacrylamide ・ N,N-Diisopropylaminoethanol ・ N,N-Diisopropylethylamine ・ N,N-Dimethyl-1-naphthylamine ・ N,N-Dimethyldopamine ・ N,N-Dimethylethylamine ・ N,N-dimethylformamidase ・ N,N-Dimethylsphingosine ・ N,N-Dimethyltryptamine ・ N,N′-Dimethyl-1,3-propanediamine ・ N,O-Dimethyl-4-(2-naphthyl)piperidine-3-carboxylate ・ N,O-Dimethylhydroxylamine ・ N- ・ N-(1-Naphthyl)ethylenediamine
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N,N'-Diisopropylcarbodiimide : ウィキペディア英語版 | N,N'-Diisopropylcarbodiimide
''N,N′''-Diisopropylcarbodiimide is a carbodiimide used in peptide synthesis. As a liquid, it is easier to handle than the commonly used ''N,N′''-dicyclohexylcarbodiimide, especially since its urea is soluble in most organic solvents, facilitating work-up. Users should be careful during handling since it is toxic and harmful to eyes. ==Further reading==
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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「N,N'-Diisopropylcarbodiimide」の詳細全文を読む
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