(2R)-3β-Ethyl-1,3,4,6,7,11bβ-hexahydro-9,10-dimethoxy-2H-benzo[a]quinolizine-2α-acetaldehyde

(2R)-3β-Ethyl-1,3,4,6,7,11bβ-hexahydro-9,10-dimethoxy-2H-benzo[a]quinolizine-2α-acetaldehyde 구조식 이미지
카스 번호:
549-91-7
상품명:
(2R)-3β-Ethyl-1,3,4,6,7,11bβ-hexahydro-9,10-dimethoxy-2H-benzo[a]quinolizine-2α-acetaldehyde
동의어(영문):
Protoemetine;(2R)-3β-Ethyl-1,3,4,6,7,11bβ-hexahydro-9,10-dimethoxy-2H-benzo[a]quinolizine-2α-acetaldehyde;2H-Benzo[a]quinolizine-2-acetaldehyde, 3-ethyl-1,3,4,6,7,11b-hexahydro-9,10-dimethoxy-, (2R,3R,11bS)-
CBNumber:
CB22195090
분자식:
C19H27NO3
포뮬러 무게:
317.42
MOL 파일:
549-91-7.mol

(2R)-3β-Ethyl-1,3,4,6,7,11bβ-hexahydro-9,10-dimethoxy-2H-benzo[a]quinolizine-2α-acetaldehyde 속성

안전

(2R)-3β-Ethyl-1,3,4,6,7,11bβ-hexahydro-9,10-dimethoxy-2H-benzo[a]quinolizine-2α-acetaldehyde C화학적 특성, 용도, 생산

개요

An oily base obtained from the bark of Cephaelis Ipecacuanha (Brot) A. Rich, the alkaloid is characterized as the perchlorate which forms crystals of the monohydrate from aqueous EtOH, m.p. 140-2°C or 193-5°C (dry). This salt has [α]D - 10.9° (c 3.13, EtOH) and gives an ultraviolet spectrum in ethanol with two absorption maxima at 232 and 283 mJ1. The base contains a formylmethyl group and yields a crystalline semicarbazone, m.p. 168-9°C. The optically inactive base has been synthesized and is also a colourless oil, giving a semicarbazone, m.p. 185-6°C.

참고 문헌

Battersby, Davidson, Harper.,J. Chem. Soc., 1744 (1959)
Battersby, Harper., ibid, 1748 (1959)
Synthesis: Santay, Toke, Kolonits., J. Org. Chem., 31, 1447 (1966)

(2R)-3β-Ethyl-1,3,4,6,7,11bβ-hexahydro-9,10-dimethoxy-2H-benzo[a]quinolizine-2α-acetaldehyde 준비 용품 및 원자재

원자재

준비 용품


(2R)-3β-Ethyl-1,3,4,6,7,11bβ-hexahydro-9,10-dimethoxy-2H-benzo[a]quinolizine-2α-acetaldehyde 공급 업체

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