(5β,12S,19β)-2,3-Didehydro-7α-ethyl-8,20,21-trinoraspidospermidine-3-carboxylic acid methyl ester

(5β,12S,19β)-2,3-Didehydro-7α-ethyl-8,20,21-trinoraspidospermidine-3-carboxylic acid methyl ester 구조식 이미지
카스 번호:
59871-84-0
상품명:
(5β,12S,19β)-2,3-Didehydro-7α-ethyl-8,20,21-trinoraspidospermidine-3-carboxylic acid methyl ester
동의어(영문):
Ibophyllidine;2,3-Didehydro-7α-ethyl-8,20,21-trinoraspidospermidine-3-carboxylic acid methyl ester;(5β,12S,19β)-2,3-Didehydro-7α-ethyl-8,20,21-trinoraspidospermidine-3-carboxylic acid methyl ester;Pyrrolizino[1,7-cd]carbazole-4-carboxylic acid, 1-ethyl-1,2,2a,3,5,10,11,12a-octahydro-, methyl ester, (1R,2aS,9bS,12aR)-
CBNumber:
CB22427702
분자식:
C20H24N2O2
포뮬러 무게:
324.42
MOL 파일:
59871-84-0.mol

(5β,12S,19β)-2,3-Didehydro-7α-ethyl-8,20,21-trinoraspidospermidine-3-carboxylic acid methyl ester 속성

안전

(5β,12S,19β)-2,3-Didehydro-7α-ethyl-8,20,21-trinoraspidospermidine-3-carboxylic acid methyl ester C화학적 특성, 용도, 생산

개요

A recent reinvestigation of the alkaloids present in the leaves of Tabernanthe iboga and T. subsessilis has resulted in the isolation of two new bases, ibophyllidine and iboxyphylline (q.v.). Ibophyllidine has been obtained as a non-crystallizable solid having no definite melting point. It is dextrorotatory with a specific rotation of [cd D + 1340 (c 1.0, CHCI3) and gives an ultraviolet spectrum in EtOH consisting of absorption maxima at 227,302 and 333 nm. The structure has been deduced primarily from a study of the ultraviolet and NMR spectra.

참고 문헌

Khuong-Huu et aZ., Tetrahedron, 32, 2539 (1976)

(5β,12S,19β)-2,3-Didehydro-7α-ethyl-8,20,21-trinoraspidospermidine-3-carboxylic acid methyl ester 준비 용품 및 원자재

원자재

준비 용품


(5β,12S,19β)-2,3-Didehydro-7α-ethyl-8,20,21-trinoraspidospermidine-3-carboxylic acid methyl ester 공급 업체

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