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・ 3-Ethylpentane
・ 3-Ethylphenol
・ 3-Faced Elva
・ 3-Fluoroamphetamine
・ 3-Fluoroethamphetamine
・ 3-Fluoromethamphetamine
・ 3-Fluoromethcathinone
・ 3-Fluorophenmetrazine
・ 3-fold
・ 3-fumarylpyruvate hydrolase
・ 3-Fumarylpyruvic acid
・ 3-galactosyl-N-acetylglucosaminide 4-alpha-L-fucosyltransferase
・ 3-Gun Nation
・ 3-Headed Shark Attack
・ 3-Heptanol
3-Heptanone
・ 3-Hexanol
・ 3-Hexanone
・ 3-hexulose-6-phosphate synthase
・ 3-Hexyne
・ 3-HO-PCP
・ 3-Hydroxy-16-methoxy-2,3-dihydrotabersonine
・ 3-hydroxy-16-methoxy-2,3-dihydrotabersonine N-methyltransferase
・ 3-hydroxy-2-methylbutyryl-CoA dehydrogenase
・ 3-hydroxy-2-methylpyridine-4,5-dicarboxylate 4-decarboxylase
・ 3-hydroxy-2-methylpyridinecarboxylate dioxygenase
・ 3-hydroxy-2-methylquinolin-4-one 2,4-dioxygenase
・ 3-hydroxy-3-isohexenylglutaryl-CoA lyase
・ 3-hydroxy-3-methylglutaryl-CoA lyase
・ 3-hydroxy-3-methylglutaryl-CoA lyase deficiency


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3-Heptanone : ウィキペディア英語版
3-Heptanone

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3-Heptanone (butyl ethyl ketone), is a seven carbon ketone. It is a colorless liquid with a "green odor," also described to have a fruity scent. It is often used as a perfume/fragrance, as a solvent for cellulose, nitrocellulose, or vinyl resins, and as a synthetic building block in the preparation of other organic molecules.
==Preparation==
3-Heptanone is produced industrially through reductive condensation of propanal with 2-butanone. This reaction does not immediately yield 3-Heptanone. Rather it results in the production of a ketone with an alkene group. This alkene can be removed with hydrogenation.
CH3CH2CHO + CH3C(O)CH2CH3 --> CH3CH2C(O)CH=CHCH2CH3 + H2 --> CH3CH2C(O)CH2CH2CH2CH3

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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