翻訳と辞書 Words near each other ・ Phenylene ・ Phenylenediamine ・ Phenylephrine ・ Phenylethanoid ・ Phenylethanolamine ・ Phenylethanolamine N-methyltransferase ・ Phenylethylidenehydrazine ・ Phenylethylmalonamide ・ Phenylethylpyrrolidine ・ Phenylglyoxal ・ Phenylglyoxylate dehydrogenase (acylating) ・ Phenylglyoxylic acid ・ Phenylhydrazine ・ Phenylhydroxylamine ・ Phenylisobutylamine ・ Phenylisocyanate ・ Phenylketonuria ・ Phenyllithium ・ Phenylmagnesium bromide ・ Phenylmercuric borate ・ Phenylmercury acetate ・ Phenylobacterium immobile ・ Phenylphosphine ・ Phenylpiperazine ・ Phenylpiperidine ・ Phenylpropanoic acid ・ Phenylpropanoid ・ Phenylpropanoids metabolism ・ Phenylpropanolamine ・ Phenylpropene Dictionary Lists mini英和辞書 mini和英辞書 Webster 1913 Latin-English FOLDOC Wikipedia English ウィキペディア

翻訳と辞書　辞書検索 [ 開発暫定版 ] スポンサード リンク Phenylisocyanate ： ウィキペディア英語版 Phenylisocyanate |Section2= |Section3= }} Phenylisocyanate is an organic compound typically abbreviated PhNCO. The molecule consists of a phenyl ring attached to the isocyanate functional group. It is a colourless liquid that reacts with water. Phenylisocyanate has a strong odor and tearing vapours, therefore it should be handled in the fumehood. Characteristic of other isocyanates, it reacts with amines to give ureas.〔Emmanuil I. Troyansky "Phenyl Isocyanate" in Encyclopedia of Reagents for Organic Synthesis, 2001 John Wiley & Sons 〕 Similarly, reacts with alcohols to form carbamates. It is used in addition with triethylamine to activate nitro groups to undergo (C,O) 1,3-dipolar cycloaddition (as opposed to O,O). The nitro group (RCH2NO2) is converted to RCNO in the reaction, with CO2 as one of the by products. == References == 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「Phenylisocyanate」の詳細全文を読む スポンサード リンク 翻訳と辞書 : 翻訳のためのインターネットリソース Copyright(C) kotoba.ne.jp 1997-2016. All Rights Reserved.