翻訳と辞書 ・ 2,2,6,6-Tetramethylpiperidine ・ 2,2-Di-2-furylpropane ・ 2,2-dialkylglycine decarboxylase (pyruvate) ・ 2,2-Dichloro-1,1,1-trifluoroethane ・ 2,2-Dimethoxy-2-phenylacetophenone ・ 2,2-Dimethoxypropane ・ 2,2-Dimethyl-1-butanol ・ 2,2-Dimethylbutane ・ 2,2-Diphenylpropylamine ・ 2,3,3,3-Tetrafluoropropene ・ 2,3,3-Trimethylpentane ・ 2,3,4,5-Tetrahydro-1,5-methano-1H-3-benzazepine ・ 2,3,4,5-tetrahydropyridine-2,6-dicarboxylate N-succinyltransferase ・ 2,3,4,5-Tetramethoxyamphetamine ・ 2,3,4-Trimethylpentane ・ 2,3,5,6,8-Pentahydroxy-1,4-naphthalenedione ・ 2,3,5,7-Tetrahydroxy-1,4-naphthalenedione ・ 2,3,7,8-Tetrachlorodibenzodioxin ・ 2,3-(S)-Hexahydroxydiphenoyl-D-glucose ・ 2,3-Bis(acetylmercaptomethyl)quinoxaline ・ 2,3-bisphosphoglycerate 3-phosphatase ・ 2,3-Bisphosphoglyceric acid ・ 2,3-Butanediol ・ 2,3-Butylene carbonate ・ 2,3-diaminopropionate N-oxalyltransferase ・ 2,3-Diaminopropionic acid ・ 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone ・ 2,3-Dichlorophenylpiperazine ・ 2,3-dihydro-2,3-dihydroxybenzoate dehydrogenase ・ 2,3-Dihydrofuran
|
|
2,3,5,6,8-Pentahydroxy-1,4-naphthalenedione : ウィキペディア英語版 | 2,3,5,6,8-Pentahydroxy-1,4-naphthalenedione
|Section2= |Section3= }} 2,3,5,6,8-Pentahydroxy-1,4-naphthalenedione, also called 2,3,5,6,8-pentahydroxy-1,4-naphthoquinone or spinochrome D, is an organic compound with formula , formally derived from 1,4-naphthoquinone through the replacement of five hydrogen atoms by hydroxyl (OH) groups. Spinochrome D occurs naturally as a brownish red pigment in the shell and spines of sea urchins such as the Japanese ''aka-uni'' (''Pseudocentrotus depressus'').〔 Chika KURODA and Masae OKAJIMA (1967), ''Studies on the Derivatives of Naphthoquinones, XVIII. The pigments of sea urchins, XIII''. Proc. Japan Acad., volume 43, pages 41--44. (Online version ) accessed on 2010-02-01. 〕 It is soluble in diethyl ether and crystallizes as brownish red needles that sublime at 285−295 °C.〔 The compound gives a yellowish brown solution when treated with sodium hydroxide, a bluish green solution with ferric chloride, and a violet precipitate with lead acetate. It forms a five-fold acetate ester, ()5, that crystallizes from methanol as yellow needles that melt at 185−186 °C.〔 == See also ==
* Hexahydroxynaphthoquinone (spinochrome E) * 2,3,5,7-Tetrahydroxy-1,4-naphthoquinone (spinochrome B)
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「2,3,5,6,8-Pentahydroxy-1,4-naphthalenedione」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.
|
|