(3β,7R,16E)-16,17-Didehydro-9-hydroxy-17-methoxy-2-oxocorynoxan-16-carboxylic acid methyl ester

(3β,7R,16E)-16,17-Didehydro-9-hydroxy-17-methoxy-2-oxocorynoxan-16-carboxylic acid methyl ester 구조식 이미지
카스 번호:
5171-42-6
상품명:
(3β,7R,16E)-16,17-Didehydro-9-hydroxy-17-methoxy-2-oxocorynoxan-16-carboxylic acid methyl ester
동의어(영문):
Speciofoline;(3β,7R,16E)-16,17-Didehydro-9-hydroxy-17-methoxy-2-oxocorynoxan-16-carboxylic acid methyl ester;Spiro[3H-indole-3,1'(5'H)-indolizine]-7'-acetic acid, 6'-ethyl-1,2,2',3',6',7',8',8'a-octahydro-4-hydroxy-α-(methoxymethylene)-2-oxo-, methyl ester, (αE,1'R,6'S,7'S,8'aR)-
CBNumber:
CB92303278
분자식:
C22H28N2O5
포뮬러 무게:
400.47
MOL 파일:
5171-42-6.mol

(3β,7R,16E)-16,17-Didehydro-9-hydroxy-17-methoxy-2-oxocorynoxan-16-carboxylic acid methyl ester 속성

녹는점
202-4°C

안전

(3β,7R,16E)-16,17-Didehydro-9-hydroxy-17-methoxy-2-oxocorynoxan-16-carboxylic acid methyl ester C화학적 특성, 용도, 생산

개요

The leaves of Mitragyna speciosa Korth contain this alkaloid which crystallizes from EtOH in colourless needles. It is laevorotatory with [α]22D - 103° (c 2.0, CHCI3). The ultraviolet spectrum has absorption maxima at 223, 242 and 290 mJ.1. The alkaloid has been shown to be a stereoisomer of rotundifoline (q.v.).

참고 문헌

Beckett, Lee, Tackie., Tetrahedron Lett., 1709 (1963)

(3β,7R,16E)-16,17-Didehydro-9-hydroxy-17-methoxy-2-oxocorynoxan-16-carboxylic acid methyl ester 준비 용품 및 원자재

원자재

준비 용품


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