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(2β,5β,12S,19β)-15-[14,15-Dihydroeburnamenin-14α-yl]-1-methylaspidofractinine-3α-carboxylic acid methyl ester

 структура
5263-34-3
CAS №
5263-34-3
английское имя:
(2β,5β,12S,19β)-15-[14,15-Dihydroeburnamenin-14α-yl]-1-methylaspidofractinine-3α-carboxylic acid methyl ester
Синонимы:
Pleiomutine;(2β,5β,12S,19β)-15-[14,15-Dihydroeburnamenin-14α-yl]-1-methylaspidofractinine-3α-carboxylic acid methyl ester;2,21-Cycloaspidospermidine-3-carboxylic acid, 15-[(14α)-14,15-dihydroeburnamenin-14-yl]-1-methyl-, methyl ester, (2β,3α)-
CBNumber:
CB72410619
Формула:
C41H50N4O2
молекулярный вес:
630.88
MOL File:
5263-34-3.mol

(2β,5β,12S,19β)-15-[14,15-Dihydroeburnamenin-14α-yl]-1-methylaspidofractinine-3α-carboxylic acid methyl ester атрибут

Температура плавления: 225°C (dec.).
плотность: 1.42±0.1 g/cm3(Predicted)
пка: 9.46±0.40(Predicted)

Заявления о рисках и безопасности

(2β,5β,12S,19β)-15-[14,15-Dihydroeburnamenin-14α-yl]-1-methylaspidofractinine-3α-carboxylic acid methyl ester химические свойства, назначение, производство

Описание

A further minor constituent of Pleiocarpa rnutica Benth, the base forms colourless crystals from CHC13-MeOH. It is strongly laevorotatory with [α]26D - 111 ° (c 1.93, CHC13), the ultraviolet spectrum in MeOH having absorption maxima at 230, 263, 285 and 292 mp.. The alkaloid is dimeric, the structure as determined from chemical analysis and spectroscopic examination being 15-( 14'- eburnamy1)p1eiocarpinine.

использованная литература

Kump, Schmid., Helv. Chirn. Acta, 44, 1503 (1961)
Structure and partial synthesis: Thomas, Achenbach, Biemann., 1. Arner. Chern. Soc., 88, 1537 (1966)

(2β,5β,12S,19β)-15-[14,15-Dihydroeburnamenin-14α-yl]-1-methylaspidofractinine-3α-carboxylic acid methyl ester препаратная продукция и сырье

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