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・ 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
・ 2-Nitrobenzaldehyde
・ 2-Nitrochlorobenzene
2-Nitrocinnamaldehyde
・ 2-Nitrodiphenylamine
・ 2-Nitrofluorene
・ 2-nitroimidazole nitrohydrolase
・ 2-nitrophenol 2-monooxygenase
・ 2-Nitropropane
・ 2-nitropropane dioxygenase
・ 2-Nitrotoluene
・ 2-Nonanol
・ 2-Nonenal
・ 2-Norbornyl cation
・ 2-Octanol
・ 2-Octyl cyanoacrylate
・ 2-OH-NPA
・ 2-Oleoylglycerol


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

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2-Nitrocinnamaldehyde, ''ortho''-nitrocinnamaldehyde or ''o''-nitrocinnamaldehyde is an organic aromatic compound containing a nitro group ortho- to the 1-position of cinnamaldehyde.
==Synthesis==

2-Nitrocinnamaldehyde can be synthesized by dissolving cinnamaldehyde to a solution of acetic anhydride in acetic acid, and adding a stoichiometric amount of concentrated nitric acid at 0–5 °C. Yields are around 36-46% of theoretical.
Nitration of cinnamaldehyde via acidification of a nitrate salt with H2SO4 also yields the ortho-nitro compound, however it also yields some of the para-nitro compound, which is generally undesired.
2-Nitrocinnamaldehyde can also be prepared by reacting 2-nitrobenzaldehyde with acetaldehyde in a condensation reaction.〔http://www.orgsyn.org/orgsyn/prep.asp?rxntypeid=181&prep=CV4P0722〕

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