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・ 2-Ethylanthraquinone
・ 2-Ethylhexanoic acid
・ 2-Ethylhexanol
・ 2-Ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine
・ 2-ethylmalate synthase
・ 2-EXPTIME
・ 2-factor theorem
・ 2-Fluoroamphetamine
・ 2-Fluoroethanol
・ 2-Fluoromethamphetamine
・ 2-Formylbenzoate dehydrogenase
・ 2-Formylpyridine
・ 2-functor
・ 2-Furanone
・ 2-furoate—CoA ligase
2-Furoic acid
・ 2-Furonitrile
・ 2-Furoyl chloride
・ 2-furoyl-CoA dehydrogenase
・ 2-graph
・ 2-group
・ 2-haloacid dehalogenase (configuration-inverting)
・ 2-haloacid dehalogenase (configuration-retaining)
・ 2-haloalkanoic acid dehalogenase
・ 2-Headed Shark Attack
・ 2-Heptanol
・ 2-Heptanone
・ 2-hexadecenal reductase
・ 2-Hexanol
・ 2-Hexanone


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

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2-Furoic acid is a heterocyclic carboxylic acid, consisting of a five-membered aromatic ring and a carboxylic acid group. Its name is derived from the Latin word ''furfur'', meaning bran.〔Alexander Senning. Elsevier's Dictionary of Chemoetymology. Elsevier, 2006. ISBN 0-444-52239-5.〕 The salts and esters of furoic acids are known as furoates.
2-Furoic acid is an organic compound most widely found in food products as a preservative and a flavoring agent. Other uses for 2-furoic acid include nylon preparation and optic technologies.
==History==
2-Furoic acid was first described by Carl Wilhelm Scheele in 1780 as the first derivative of the compound furan. Since then, the compound's reactivity with different substances and organisms was tested. It was discovered that 2-furoic acid can be the sole source of carbon and energy for the organism ''Pseudomonas putida''. The organism aerobically degrades the compound.



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