(16R)-18,19-Didehydro-17-hydroxycorynan-16-carboxylic acid methyl ester

(16R)-18,19-Didehydro-17-hydroxycorynan-16-carboxylic acid methyl ester 구조식 이미지
카스 번호:
1245-00-7
상품명:
(16R)-18,19-Didehydro-17-hydroxycorynan-16-carboxylic acid methyl ester
동의어(영문):
Sitsirikin;Sitsirikine;16R-sitsirikine;(16R)-18,19-Didehydro-17-hydroxycorynan-16-carboxylic acid methyl ester;(16R)-18,19-Didehydro-17-hydroxy-17,18-secoyohimban-16-carboxylic acid methyl ester;Indolo[2,3-a]quinolizine-2-acetic acid, 3-ethenyl-1,2,3,4,6,7,12,12b-octahydro-α-(hydroxymethyl)-, methyl ester, (αR,2S,3R,12bS)-
CBNumber:
CB22320562
분자식:
C21H26N2O3
포뮬러 무게:
354.45
MOL 파일:
1245-00-7.mol

(16R)-18,19-Didehydro-17-hydroxycorynan-16-carboxylic acid methyl ester 속성

녹는점
239-241℃ (Decomposition)
끓는 점
545.4±50.0 °C(Predicted)
밀도
1.25±0.1 g/cm3(Predicted)
산도 계수 (pKa)
14.30±0.10(Predicted)

안전

(16R)-18,19-Didehydro-17-hydroxycorynan-16-carboxylic acid methyl ester C화학적 특성, 용도, 생산

개요

One of the numerous alkaloids isolated from Vinca species, this base occurs in V. rosea L. and forms colourless crystals from MeOH. It is laevorotatory with[α]26D - 58° (MeOH) and when crystallized from Me2CO forms crystals containing solvent of crystallization, m.p. 181°C. The ultraviolet spectrum in MeOH has absorption maxima at 226, 282 and 290 mf.1. The alkaloid contains a primary alcoholic group and an imino group and yields the hemisulphate, m.p. 239- 241°C (dec.); the picrate, m.p. 226-8°C (dec.) and the O-acetate, m.p. 198°C;[α]26D- 26° (MeOH).

참고 문헌

Svoboda et al., J. Pharm. Sci., 50,409 (1961)
Kutney, Brown., Tetrahedron Lett., 1815 (1963)

(16R)-18,19-Didehydro-17-hydroxycorynan-16-carboxylic acid methyl ester 준비 용품 및 원자재

원자재

준비 용품


(16R)-18,19-Didehydro-17-hydroxycorynan-16-carboxylic acid methyl ester 공급 업체

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