(2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol

(2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol 구조식 이미지
카스 번호:
6582-68-9
상품명:
(2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol
동의어(영문):
Kopsanol;(22S)-Kopsan-22-ol;(2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol;6H,13aH-3a,5a-Ethano-5,11-methano-1H-indolizino[8,1-cd]carbazol-14-ol, 2,3,4,5,11,12-hexahydro-, (3aR,5R,5aR,10bR,11R,13aS,14S)-
CBNumber:
CB32193497
분자식:
C20H24N2O
포뮬러 무게:
308.42
MOL 파일:
6582-68-9.mol

(2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol 속성

녹는점
239-245°C (dec.).

안전

(2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol C화학적 특성, 용도, 생산

개요

An imidazolidinocarbazole alkaloid, this base occurs in Aspidosperma duckei Hub. and also in A. macrocarpon Mart. It may be purified by recrystallization from either MeOH or CHC1 3 when it forms colourless needles. It has [α]27D + 16.7° (c 0.6, CHC13 ). The ultraviolet spectrum in ethanol solution has absorp-tion maxima at 246 and 297 mil. In 5N/HCl the absorption maxima occur at 262 and 268.5 mil with shoulders at 249 and 255 mil. The alkaloid contains one hydroxyl group and on acetylation yields the O-acetate, m.p. 202-5°C; [α]26D + 37° (c 2.97, CHCI3 ).

참고 문헌

Filho et al., J. Chem. Soc., C, 1260 (1966)

(2R,3R,5R,11S,22S)-3,11-Methanoaspidofractinin-22-ol 준비 용품 및 원자재

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