이소마하니빈

이소마하니빈 C화학적 특성, 용도, 생산

개요

The roots and leaves of Murraya koenigii Spreng. yield this alkaloid which is best crystallized from CH2 C1r hexane. It has [α]_D - 6° (c 2.01, CHC1 3 ) and the ultraviolet spectrum in EtOH shows absorption maxima at 225, 278, 281, 295, 335 and 354 mp. Catalytic hydrogenation with Pd-C gives the tetrahydro deriva_x0002_tive, m.p. l66-7°C, as colourless crystals from pentane, the ultraviolet spectrum of which has absorption maxima at 220, 241, 255,260,306 and 320 mp. Treatment with methyl sulphate in NaOH yields the N-methyl compound, m.p. 94°C, giving an ultraviolet spectrum in EtOH consisting of absorption maxima at 240, 293,332,345 and 358 mp.

참고 문헌

Joshi, Kamat, Gawad., Tetrahedron, 26, 1475 (1970)

이소마하니빈 준비 용품 및 원자재

원자재

준비 용품

이소마하니빈 공급 업체

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