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・ 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
・ 2-Naphthol
・ 2-Naphthylamine
・ 2-Nitroaniline


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

2-Methylimidazole is an organic compound that is structurally related to imidazole with the chemical formula CH3C3H2N2H. It is a white or colorless solid that is highly soluble in polar organic solvents. It is a precursor to a range of drugs and is a ligand in coordination chemistry.
==Synthesis and reactions==
It is prepared by condensation of glyoxal, ammonia, and acetaldehyde, a Radziszewski reaction. Nitration gives 5-nitro derivative.〔Ebel, K., Koehler, H., Gamer, A. O., & Jäckh, R. "Imidazole and Derivatives." In Ullmann’s Encyclopedia of Industrial Chemistry; 2002 Wiley-VCH, 〕
2-Methylimidazole is a sterically hindered imidazole that is used to similuate the coordination of histidine to heme complexes. It can be deprotonated to make imidazolate-based coordination polymers.

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