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・ Trifurcula iberica
・ Trifurcula immundella
・ Trifurcula istriae
・ Trifurcula josefklimeschi
・ Trifurcula kalavritana
・ Trifurcula lavandulae
・ Trifurcula liskai
・ Trifurcula luteola
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・ Trifluoromethanesulfonic acid
・ Trifluoromethanesulfonic anhydride
・ Trifluoromethanesulfonyl azide
・ Trifluoromethyl
Trifluoromethyl hypofluorite
・ Trifluoromethyl sulphur pentafluoride
・ Trifluoromethylaminoindane
・ Trifluoromethylation
・ Trifluoromethylisocyanide
・ Trifluoromethylphenylpiperazine
・ Trifluoromethylsulfonyl
・ Trifluoromethyltrimethylsilane
・ Trifluorooxonium
・ Trifluorotoluene
・ Trifluperidol
・ Triflupromazine
・ Trifluralin
・ Trifluridine
・ Trifluridine/tipiracil


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Trifluoromethyl hypofluorite : ウィキペディア英語版
Trifluoromethyl hypofluorite

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Trifluoromethyl hypofluorite is an organofluorine compound with the formula . It exists as a colorless gas at room temperature and is highly toxic. It is a rare example of a hypofluorite (compound with an O-F bond). It is prepared by the fluorination of carbon monoxide:
:2 F2 + CO → CF3OF
The gas hydrolyzes only slowly at neutral pH.
==Use in organic chemistry==
The compound is a source of electrophilic fluorine. It has been used for the preparation of α-fluoroketones from silyl enol ethers.
Behaving like a pseudohalogen, it adds to ethylene to give the ether:
:CF3OF + CH2CH2 → CF3OCH2CH2F

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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