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・ 1-K pot
・ 1-Lysophosphatidylcholine
・ 1-Meg Modem
・ 1-Methyl-5-methoxy-diisopropyltryptamine
・ 1-methyladenosine nucleosidase
・ 1-Methylamino-1-(3,4-methylenedioxyphenyl)propane
・ 1-Methylcyclopropene
・ 1-Methylimidazole
・ 1-Methylindole
・ 1-Methylnaphthalene
・ 1-Methylpsilocin
・ 1-Methyltryptophan
・ 1-millimeter band
・ 1-Naphthaleneacetamide
・ 1-Naphthaleneacetic acid
1-Naphthol
・ 1-Naphthyl isothiocyanate
・ 1-Naphthylamine
・ 1-Nitropropane
・ 1-Nitropyrene
・ 1-Nonacosanol
・ 1-Nonanol
・ 1-Nonyl-4-phenol
・ 1-Nonylnaphthalene
・ 1-NP
・ 1-Octacosanol
・ 1-Octanol
・ 1-Octen-3-ol
・ 1-Octen-3-yl acetate
・ 1-Octene


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1-Naphthol : ウィキペディア英語版
1-Naphthol

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1-Naphthol, or α-naphthol, is a fluorescent organic compound with the formula C10H7OH. It is a white solid. It is an isomer of 2-naphthol differing by the location of the hydroxyl group on the naphthalene ring. The naphthols are naphthalene homologues of phenol, with the hydroxyl group being more reactive than in the phenols. Both isomers are soluble in simple alcohols, ethers, and chloroform. They are precursors to a variety of useful compounds. Naphthols (both 1 and 2 isomers) are used as biomarkers for livestock and humans exposed to polycyclic aromatic hydrocarbons.
==Production==
1-Naphthol is prepared by two main routes.〔 In one method, naphthalene is nitrated to give 1-nitronaphthalene, which is hydrogenated to the amine followed by hydrolysed:
: C10H8 + HNO3 → C10H7NO2 + H2O
: C10H7NO2 + 3 H2 → C10H7NH2 + 2 H2O
: C10H7NH2 + H2O → C10H7OH + NH3
Alternatively, naphthalene is hydrogenated to tetralin, which is oxidized to 1-tetralone, which undergoes dehydrogenation.

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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