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(16R)-17-Acetyloxy-10-methoxyakuammilan-16-carboxylic acid methyl ester

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(16R)-17-Acetyloxy-10-methoxyakuammilan-16-carboxylic acid methyl ester Basic information
Product Name:(16R)-17-Acetyloxy-10-methoxyakuammilan-16-carboxylic acid methyl ester
Synonyms:(16R)-17-Acetyloxy-10-methoxyakuammilan-16-carboxylic acid methyl ester;10-Methoxyakuammiline;Raufloricine
CAS:38734-62-2
MF:C24H28N2O5
MW:424.48952
EINECS:
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Mol File:38734-62-2.mol
(16R)-17-Acetyloxy-10-methoxyakuammilan-16-carboxylic acid methyl ester Structure
(16R)-17-Acetyloxy-10-methoxyakuammilan-16-carboxylic acid methyl ester Chemical Properties
Melting point 190-2°C
Safety Information
MSDS Information
(16R)-17-Acetyloxy-10-methoxyakuammilan-16-carboxylic acid methyl ester Usage And Synthesis
DescriptionThe root bark of Rauwolfia confertiflora Pichon yields this alkaloid which forms colourless crystals from AcOEt. The base is strongly dextrorotatory with [α]20D + 129° (c l.5, CHCI3). In MeOH, the ultraviolet spectrum exhibits absorption maxima at 225,286 and 310 ffiJ.1. The alkaloid has been shown to be pentacyclic and contains a methoxyl group, an allyl group, a methoxycarbonyl and an acetoxymethyl group.
ReferencesDanieli et ai., Chern. Ind. (Milan), 54, 618 (1972)
(16R)-17-Acetyloxy-10-methoxyakuammilan-16-carboxylic acid methyl ester Preparation Products And Raw materials
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