翻訳と辞書 ・ 1,2-Wittig rearrangement
・ 1,227 QI Facts to Blow Your Socks Off
・ 1,3,2,4-Dithiadiphosphetane 2,4-disulfides
・ 1,3,3,3-Tetrafluoropropene
・ 1,3,5-Triazido-2,4,6-trinitrobenzene
・ 1,3,5-Triazine
・ 1,3,5-Trichlorobenzene
・ 1,3,5-Trinitrobenzene
・ 1,3,5-Trioxane
・ 1,3,5-Trioxanetrione
・ 1,3,5-Trithiane
・ 1,3,6-Trigalloyl glucose
・ 1,3,7-Trimethyluric acid
・ 1,3,8-Trihydroxyanthraquinone
・ 1,3-alpha-L-fucosidase
・ 1,3-Benzodioxole
・ 1,3-Benzodioxolyl-N-ethylbutanamine
・ 1,3-Benzodioxolyl-N-ethylpentanamine
・ 1,3-Benzodioxolyl-N-methylbutanamine
・ 1,3-Benzodioxolyl-N-methylpentanamine
・ 1,3-Benzodioxolylbutanamine
・ 1,3-beta-D-glucan phosphorylase
・ 1,3-beta-galactosyl-N-acetylhexosamine phosphorylase
・ 1,3-Beta-glucan synthase
・ 1,3-beta-oligoglucan phosphorylase
・ 1,3-Bis(dicyanomethylene)squarate
・ 1,3-Bis(diphenylphosphino)propane
・ 1,3-Bisphosphoglyceric acid
・ 1,3-Butadiene
・ 1,3-Butadiene (data page)
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| 1,3-Benzodioxole ： ウィキペディア英語版 |
1,3-Benzodioxole
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1,3-Benzodioxole (1,2-methylenedioxybenzene) is an organic compound with the formula C6H4O2CH2. The compound is classified as benzene derivative and a heterocyclic compound containing the methylenedioxy functional group. It is a colorless liquid.
Although benzodioxozole is not particularly important, many related compounds containing the methylenedioxyphenyl group are bioactive, and thus are found in pesticides and pharmaceuticals.〔Murray, M., "Mechanisms of inhibitory and regulatory effects of methylenedioxyphenyl compounds on cytochrome P450-dependent drug oxidation", Curr. Drug Metab. 2000, volume 1, 67-84. 〕
==Preparation==
1,3-Benzodioxole can be synthesized from catechol with disubstituted halomethanes.
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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