6-메톡시-1,3-디옥솔로[4,5-h]푸로[2,3-b]퀴놀린

6-메톡시-1,3-디옥솔로[4,5-h]푸로[2,3-b]퀴놀린
6-메톡시-1,3-디옥솔로[4,5-h]푸로[2,3-b]퀴놀린 구조식 이미지
카스 번호:
482-32-6
한글명:
6-메톡시-1,3-디옥솔로[4,5-h]푸로[2,3-b]퀴놀린
동의어(한글):
6-메톡시-1,3-디옥솔로[4,5-h]푸로[2,3-b]퀴놀린
상품명:
6-Methoxy-1,3-dioxolo[4,5-h]furo[2,3-b]quinoline
동의어(영문):
Kokusagine;6-Methoxy-1,3-dioxolo[4,5-h]furo[2,3-b]quinoline;1,3-Dioxolo[4,5-h]furo[2,3-b]quinoline, 6-methoxy-
CBNumber:
CB92359826
분자식:
C13H9NO4
포뮬러 무게:
243.21
MOL 파일:
482-32-6.mol

6-메톡시-1,3-디옥솔로[4,5-h]푸로[2,3-b]퀴놀린 속성

녹는점
194°C
끓는 점
408.7±40.0 °C(Predicted)
밀도
1.440±0.06 g/cm3(Predicted)
산도 계수 (pKa)
7.18±0.20(Predicted)

안전

6-메톡시-1,3-디옥솔로[4,5-h]푸로[2,3-b]퀴놀린 C화학적 특성, 용도, 생산

개요

Terasaka has isolated this furoquinoline alkaloid from the roots of Orixa japonica and Obata has found that it also occurs in the fruit along with skim_x0002_mianine (q.v.). The alkaloid is optically inactive and is converted by Mel at 100°C into isokokusagine, m.p. 247°C. The aurichloride has m.p. 171°C and the picrate, m.p. 178°C (157°C according to Obata). The structure has been established by synthesis as 7: 8-methylenedioxydictamnine.

참고 문헌

Terasaka.,J. Pharm. Soc. Japan, 51,99 (1931)
Obata., ibid, 59,136 (1939)
Structure:
Terasaka et at., Chem. Pharm. Bull. (Tokyo), 2, 159 (1954)

6-메톡시-1,3-디옥솔로[4,5-h]푸로[2,3-b]퀴놀린 준비 용품 및 원자재

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