propenylaminen.

Brit.

/ˌprəʊpᵻˈnʌɪləmiːn/, U.S.

/ˌproʊpəˈnaɪləˌmin/

Origin: Formed within English, by compounding. Etymons: propenyl n., amine n.

Etymology: < propenyl n. + amine n.

Chemistry.

A pale yellow liquid amine, (= allylamine n.); any compound in which an amine group is bonded to a (substituted) propenyl group.Formula: CH₂=CHCH₂NH₂.

ΚΠ

1894 H. F. Morley & M. M. P. Muir Watts' Dict. Chem. (rev. ed.) IV. 309/2 Propenylamine, formed by the action of baryta on β-bromo-propylamine.

1966 Jrnl. Org. Chem. 31 3715/2 Price and Snyder have demonstrated that propenylamines are highly favored over allylamines in base catalyzed equilibria.

1998 Jrnl. Amer. Chem. Soc. 120 158/1 The competition largely favors the isomerization of the distonic ion 2 to ionized propenylamine 3.

This entry has been updated (OED Third Edition, June 2007; most recently modified version published online March 2022).

单词	propenylamine
释义	propenylaminen. Brit. /ˌprəʊpᵻˈnʌɪləmiːn/, U.S. /ˌproʊpəˈnaɪləˌmin/ Origin: Formed within English, by compounding. Etymons: propenyl n., amine n. Etymology: < propenyl n. + amine n. Chemistry. A pale yellow liquid amine, (= allylamine n.); any compound in which an amine group is bonded to a (substituted) propenyl group.Formula: CH₂=CHCH₂NH₂. ΚΠ 1894 H. F. Morley & M. M. P. Muir Watts' Dict. Chem. (rev. ed.) IV. 309/2 Propenylamine, formed by the action of baryta on β-bromo-propylamine. 1966 Jrnl. Org. Chem. 31 3715/2 Price and Snyder have demonstrated that propenylamines are highly favored over allylamines in base catalyzed equilibria. 1998 Jrnl. Amer. Chem. Soc. 120 158/1 The competition largely favors the isomerization of the distonic ion 2 to ionized propenylamine 3. This entry has been updated (OED Third Edition, June 2007; most recently modified version published online March 2022). < n.1894
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