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・ 1,4-Cyclohexanedione
・ 1,4-Diamino-2,3-dihydroanthraquinone
・ 1,4-Diazepine
・ 1,4-Dibromobenzene
・ 1,4-Dichloro-2-nitrobenzene
・ 1,4-Dichlorobenzene
・ 1,4-Dichlorobut-2-ene
・ 1,4-dihydroxy-2-naphthoate polyprenyltransferase
・ 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


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1,4-Naphthoquinone : ウィキペディア英語版
1,4-Naphthoquinone

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1,4-Naphthoquinone or para-naphthoquinone is an organic compound derived from naphthalene. Several isomeric naphthoquinones are known, notably 1,2-naphthoquinone. 1,4-Naphthoquinone forms volatile yellow triclinic crystals and has a sharp odor similar to benzoquinone. It is almost insoluble in cold water, slightly soluble in petroleum ether, and more soluble in polar organic solvents. In alkaline solutions it produces a reddish-brown color. Vitamin K is a derivative of 1,4-naphthoquinone. It is a planar molecule with one aromatic ring fused to a quinone subunit.
==Preparation==
The industrial synthesis involves aerobic oxidation of naphthalene over a vanadium oxide catalyst:
:C10H8 + 3/2 O2 → C10H6O2 + H2O
In the laboratory, naphthoquinone can be produced by the oxidation of a variety of naphthalene compounds. An inexpensive route involves oxidation of naphthalene with chromium trioxide.

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