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・ 1,4-dihydroxy-2-naphthoyl-CoA hydrolase
・ 1,4-Dihydroxyanthraquinone
・ 1,4-Dimethoxybenzene
・ 1,4-Dioxane
・ 1,4-Dioxene
・ 1,4-Dioxin
・ 1,4-lactonase
・ 1,4-Naphthoquinone
・ 1,4-Thiazepine
・ 1,5-anhydro-D-fructose dehydratase
・ 1,5-anhydro-D-fructose reductase
・ 1,5-anhydro-D-fructose reductase (1,5-anhydro-D-mannitol-forming)
・ 1,5-Anhydroglucitol
・ 1,5-Cyclooctadiene
・ 1,5-Diazabicyclo(4.3.0)non-5-ene
1,5-Dihydroxynaphthalene
・ 1,5-Methano(10)annulene
・ 1,5-Pentanediol
・ 1,6-alpha-D-mannosidase
・ 1,6-alpha-L-fucosidase
・ 1,6-Digalloyl glucose
・ 1,6-dihydroxycyclohexa-2,4-diene-1-carboxylate dehydrogenase
・ 1,6-Hexanediol
・ 1,6-Methano(10)annulene
・ 1,68
・ 1,7-Bis(4-hydroxyphenyl)-1,4,6-heptatrien-3-one
・ 1,778 Stories of Me and My Wife
・ 1,8-Bis(dimethylamino)naphthalene
・ 1,8-Cineole 2-endo-monooxygenase
・ 1,8-Cineole 2-exo-monooxygenase


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1,5-Dihydroxynaphthalene : ウィキペディア英語版
1,5-Dihydroxynaphthalene

1,5-Dihydroxynaphthalene is an organic compound with the formula C10H6(OH)2. It is one of several isomers of dihydroxynaphthalene. It exists as colorless crystals that are soluble in polar organic solvents. It is a precursor to certain dyes.
==Preparation and use==
1,5-Dihydroxynaphthalene is prepared from naphthalene-1,5-disulfonic acid by hydrolysis with strong base followed by acidification.
It couples with various aryl diazonium salts to give diazo dyes. Oxidation with chromium trioxide gives juglone, a naturally occurring dye.〔Gerald Booth "Naphthalene Derivatives" in ''Ullmann's Encyclopedia of Industrial Chemistry'', 2005, Wiley-VCH, Weinheim. .〕

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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