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(20S)-3β-(Dimethylamino)-4,4,14-trimethyl-20-(methylamino)-B(9a)-homo-19-nor-5α-pregna-9(11),9a-dien-16α-ol

 структура
58672-77-8
CAS №
58672-77-8
английское имя:
(20S)-3β-(Dimethylamino)-4,4,14-trimethyl-20-(methylamino)-B(9a)-homo-19-nor-5α-pregna-9(11),9a-dien-16α-ol
Синонимы:
Buxaminol B;(20S)-3β-(Dimethylamino)-4,4,14-trimethyl-20-(methylamino)-B(9a)-homo-19-nor-5α-pregna-9(11),9a-dien-16α-ol;Benzo[4,5]cyclohept[1,2-e]inden-2-ol, 9-(dimethylamino)-1,2,3,3a,4,7,8,9,10,10a,11,12,12a,12b-tetradecahydro-3a,10,10,12b-tetramethyl-3-[(1S)-1-(methylamino)ethyl]-, (2R,3S,3aR,9S,10aR,12aR,12bS)-
CBNumber:
CB72247972
Формула:
C27H46N2O
молекулярный вес:
414.67
MOL File:
58672-77-8.mol

(20S)-3β-(Dimethylamino)-4,4,14-trimethyl-20-(methylamino)-B(9a)-homo-19-nor-5α-pregna-9(11),9a-dien-16α-ol атрибут

Заявления о рисках и безопасности

(20S)-3β-(Dimethylamino)-4,4,14-trimethyl-20-(methylamino)-B(9a)-homo-19-nor-5α-pregna-9(11),9a-dien-16α-ol химические свойства, назначение, производство

Описание

This alkaloid occurs in Buxus sernpervirens var. bullatus and forms colourless needles from Me2CO. It is dextrorotatory with a specific rotation of [α]D25 + 20° (c 0.59, MeOH) and gives an ultraviolet spectrum in EtOH with absorption maxima at 236, 246, 255 and 273 nm. Treatment with methyl iodide yields buxaminol A.

использованная литература

Bauerova, Paulik, Collect. Czech. Chern. Cornrnun., 40, 3055 (1975)

(20S)-3β-(Dimethylamino)-4,4,14-trimethyl-20-(methylamino)-B(9a)-homo-19-nor-5α-pregna-9(11),9a-dien-16α-ol препаратная продукция и сырье

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(20S)-3β-(Dimethylamino)-4,4,14-trimethyl-20-(methylamino)-B(9a)-homo-19-nor-5α-pregna-9(11),9a-dien-16α-ol поставщик

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