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・ 2-Methyl-3-phenylpiperidine
・ 2-Methyl-5-hydroxytryptamine
・ 2-Methyl-6-(phenylethynyl)pyridine
・ 2-Methyl-6-nitrobenzoic anhydride
・ 2-methyl-branched-chain-enoyl-CoA reductase
・ 2-Methyl-MDA
・ 2-Methylacetoacetyl-CoA
・ 2-methylacetoacetyl-CoA thiolase
・ 2-methylacyl-CoA dehydrogenase
・ 2-Methylbutyryl-CoA
・ 2-Methylbutyryl-CoA dehydrogenase deficiency
・ 2-methylcitrate dehydratase
・ 2-methylcitrate dehydratase (2-methyl-trans-aconitate forming)
・ 2-methylcitrate synthase
・ 2-methyleneglutarate mutase
2-Methylfuran
・ 2-Methylheptane
・ 2-Methylhexane
・ 2-Methylimidazole
・ 2-Methylindole
・ 2-Methylisoborneol
・ 2-methylisoborneol synthase
・ 2-methylisocitrate dehydratase
・ 2-Methylnaphthalene
・ 2-Methylpentane
・ 2-Methylphenethylamine
・ 2-Methylpyridine
・ 2-Methyltetrahydrofuran
・ 2-Methylundecanal
・ 2-millimeter band


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2-Methylfuran : ウィキペディア英語版
2-Methylfuran

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2-Methylfuran is a flammable, water-insoluble liquid〔
(【引用サイトリンク】title=Chemical Database - 2-Methylfuran. EnvironmentalChemistry.com. 1995 - 2008. Accessed on-line: 8/26/2008 )〕 with a chocolate odor, found naturally in Myrtle and Dutch Lavender
(【引用サイトリンク】title=Dr. Duke's Phytochemical and Ethnobotanical Databases. (Database ) 26 August 2008. 2-METHYL-FURAN )〕
used as a FEMA GRAS flavoring substance,〔
(【引用サイトリンク】title=2-methyl furan )〕 with the potential for use in alternative fuels.
==Manufacture==
2-Methylfuran is an article of commerce (chemical intermediate) and is normally manufactured by catalytic hydrogenolyis of furfuryl alcohol or via a hydrogenation-hydrogenolysis sequence from furfural in the vapor phase.〔L. W. Burnette, et al., "Production of 2-Methylfuran by Vapor Phase Hydrogenation of Furfural" Industrial and engineering Chemistry, V40, P502-505 (1948).〕

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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