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・ Tetrahydrocoptisine
・ Tetrahydrocorticosterone
・ Tetrahydrocortisol
・ Tetrahydrocortisone
・ Tetrahydrodeoxycorticosterone
・ Tetrahydrodipicolinate N-acetyltransferase
・ Tetrahydrofolate riboswitch
・ Tetrahydrofolate synthase
・ Tetrahydrofolic acid
・ Tetrahydrofuran
・ Tetrahydrofuran (data page)
・ Tetrahydrogestrinone
・ Tetrahydroharman
・ Tetrahydroharmine
・ Tetrahydroharmol
Tetrahydroisoquinoline
・ Tetrahydromethanopterin
・ Tetrahydromethanopterin S-methyltransferase
・ Tetrahydropalmatine
・ Tetrahydroprogesterone
・ Tetrahydropyran
・ Tetrahydrosarcinapterin synthase
・ Tetrahydrothiophene
・ Tetrahydroxy-1,4-benzoquinone
・ Tetrahydroxy-1,4-benzoquinone biscarbonate
・ Tetrahydroxy-1,4-benzoquinone bisoxalate
・ Tetrahydroxyanthraquinone
・ Tetrahydroxyborate
・ Tetrahydroxyflavone
・ Tetrahydroxynaphthalene reductase


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Tetrahydroisoquinoline : ウィキペディア英語版
Tetrahydroisoquinoline

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Tetrahydroisoquinoline is an organic compound with the chemical formula C9H11N. Classified as a secondary amine, it is derived from isoquinoline by hydrogenation. It is a colorless viscous liquid that is miscible with most organic solvents. The tetrahydroisoquinoline skeleton is encountered in a number of bioactive compounds and drugs.〔Mitchinson, Andrew; Nadin, Alan "Saturated nitrogen heterocycles" Perkin 1 2000, pp. 2862-2892. 〕
==Reactions==
As a secondary amine, tetrahydroisoquinoline has weakly basic properties and forms salts with strong acids. It can be dehydrogenated to give isoquinoline and hydrogenated to decahydroisoquinoline. Like other secondary amines, tetrahydroisoquinoline can be oxidized to the corresponding nitrone using hydrogen peroxide, catalyzed by selenium dioxide.

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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