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・ 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
・ 2-hydroxy-1,4-benzoquinone reductase
・ 2-Hydroxy-1,4-benzoxazin-3-one monooxygenase


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

2-Furoyl chloride is a corrosive liquid boiling at 173 °C, which is more irritating to the eyes than benzoyl chloride. 2-Furoyl chloride is a useful pharmaceutical intermediate and is used in the synthesis of mometasone furoate, an antiinflammatory prodrug used in the treatment of skin disorders, hay fever and asthma.〔William Heggie, "Process for the preparation of mometasone furoate", US Patent 6,177,560 B1(2001)〕
== Synthesis ==

2-Furoyl chloride was prepared in 1924 by Gelissen by refluxing 2-furoic acid in excess thionyl chloride on a water bath.〔

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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