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・ Acetoxyacetylaminofluorene
・ Acetoxybutynylbithiophene deacetylase
・ Acetoxycycloheximide
・ Acetoxyketobemidone
・ Acetrax
・ Acetrizoic acid
・ Acetropis gimmerthalii
・ Aceturic acid
・ Acetyl
・ Acetyl activating enzyme
・ Acetyl bromide
・ Acetyl chloride
・ Acetyl cyanide
・ Acetyl fluoride
・ Acetyl hexapeptide-3
Acetyl iodide
・ Acetyl tributyl citrate
・ Acetyl-CoA
・ Acetyl-CoA C-acetyltransferase
・ Acetyl-CoA C-myristoyltransferase
・ Acetyl-CoA carboxylase
・ Acetyl-CoA hydrolase
・ Acetylacetone
・ Acetylacetone-cleaving enzyme
・ Acetylajmaline esterase
・ Acetylalkylglycerol acetylhydrolase
・ Acetylated distarch adipate
・ Acetylated lanolin alcohol
・ Acetylated wood
・ Acetylation


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Acetyl iodide : ウィキペディア英語版
Acetyl iodide

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Acetyl iodide is an organoiodine compound with the formula CH3C(O)I. It is a colourless liquid. It is formally derived from acetic acid. Although far rarer in the laboratory than the related acetyl bromide and acetyl chloride, acetyl iodide is produced, transiently at least, on a far larger scale than any other acid halide. Specifically, it is generated by the carbonylation of methyl iodide in the Cativa and Monsanto processes that are the main industrial route to acetic acid. It is also an intermediate in the production of acetic anhydride from methyl acetate.
Upon treatment with carboxylic acids, acetyl iodide does not exhibit reactions typical of acyl halides, such as acetyl chloride. Instead, acetyl iodide undergoes iodide/hydroxide exchange with most carboxylic acids:

:CH3C(O)I + RCO2H → CH3CO2H + RC(O)I
== References ==


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