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(14S,20R)-4,21-Dimethyl-16-methylene-14,20-cycloveatchane-2α,5,6α,11α,12α-pentol 11,12-bis[(E)-2-methyl-2-butenoate]

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(14S,20R)-4,21-Dimethyl-16-methylene-14,20-cycloveatchane-2α,5,6α,11α,12α-pentol 11,12-bis[(E)-2-methyl-2-butenoate] Basic information
Product Name:(14S,20R)-4,21-Dimethyl-16-methylene-14,20-cycloveatchane-2α,5,6α,11α,12α-pentol 11,12-bis[(E)-2-methyl-2-butenoate]
Synonyms:(14S,20R)-4,21-Dimethyl-16-methylene-14,20-cycloveatchane-2α,5,6α,11α,12α-pentol 11,12-bis[(E)-2-methyl-2-butenoate];Anopterine
CAS:38826-62-9
MF:C31H43NO7
MW:541.681
EINECS:
Product Categories:
Mol File:38826-62-9.mol
(14S,20R)-4,21-Dimethyl-16-methylene-14,20-cycloveatchane-2α,5,6α,11α,12α-pentol 11,12-bis[(E)-2-methyl-2-butenoate] Structure
(14S,20R)-4,21-Dimethyl-16-methylene-14,20-cycloveatchane-2α,5,6α,11α,12α-pentol 11,12-bis[(E)-2-methyl-2-butenoate] Chemical Properties
Melting point 222-3°C
Safety Information
MSDS Information
(14S,20R)-4,21-Dimethyl-16-methylene-14,20-cycloveatchane-2α,5,6α,11α,12α-pentol 11,12-bis[(E)-2-methyl-2-butenoate] Usage And Synthesis
DescriptionA complex alkaloid obtained from Anopterus macleaynus F. Muell and subsequently from A. glandulosus Labill. The base is laevorotatory with a specific rotation of [α]D - 12° (c 1.47, CHC13). The structure has been established by chemical and spectroscopic methods.
DefinitionChEBI: Anopterine is a fatty acid ester.
ReferencesDenne et al., Tetrahedron Lett., 2727 (1972)
(14S,20R)-4,21-Dimethyl-16-methylene-14,20-cycloveatchane-2α,5,6α,11α,12α-pentol 11,12-bis[(E)-2-methyl-2-butenoate] Preparation Products And Raw materials
Tag:(14S,20R)-4,21-Dimethyl-16-methylene-14,20-cycloveatchane-2α,5,6α,11α,12α-pentol 11,12-bis[(E)-2-methyl-2-butenoate](38826-62-9) Related Product Information
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