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(13α,17α)-7α-Acetoxy-21,23-epoxy-4,4,8-trimethyl-24-nor-5α-chola-1,14,20,22-tetren-3-one

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(13α,17α)-7α-Acetoxy-21,23-epoxy-4,4,8-trimethyl-24-nor-5α-chola-1,14,20,22-tetren-3-one Basic information
Product Name:(13α,17α)-7α-Acetoxy-21,23-epoxy-4,4,8-trimethyl-24-nor-5α-chola-1,14,20,22-tetren-3-one
Synonyms:(13α,17α)-7α-Acetoxy-21,23-epoxy-4,4,8-trimethyl-24-nor-5α-chola-1,14,20,22-tetren-3-one;Azadirone;24-Norchola-1,14,20,22-tetraen-3-one, 7-(acetyloxy)-21,23-epoxy-4,4,8-trimethyl-, (5α,7α,13α,17α)-
CAS:25279-67-8
MF:C28H36O4
MW:436.59
EINECS:
Product Categories:
Mol File:25279-67-8.mol
(13α,17α)-7α-Acetoxy-21,23-epoxy-4,4,8-trimethyl-24-nor-5α-chola-1,14,20,22-tetren-3-one Structure
(13α,17α)-7α-Acetoxy-21,23-epoxy-4,4,8-trimethyl-24-nor-5α-chola-1,14,20,22-tetren-3-one Chemical Properties
Melting point 123-125 °C
Boiling point 506.5±50.0 °C(Predicted)
density 1.15±0.1 g/cm3(Predicted)
Safety Information
MSDS Information
(13α,17α)-7α-Acetoxy-21,23-epoxy-4,4,8-trimethyl-24-nor-5α-chola-1,14,20,22-tetren-3-one Usage And Synthesis
DefinitionChEBI: A tetracyclic triterpenoid that is 4,4,8-trimethylandrosta-1,14-diene substituted by an oxo group at position 3, an acetoxy group at position 7 and a furan-3-yl group at position 17. Isolated from Azadirachta indica, it exhibits antiplasmodial and antineoplastic activities.
(13α,17α)-7α-Acetoxy-21,23-epoxy-4,4,8-trimethyl-24-nor-5α-chola-1,14,20,22-tetren-3-one Preparation Products And Raw materials
Tag:(13α,17α)-7α-Acetoxy-21,23-epoxy-4,4,8-trimethyl-24-nor-5α-chola-1,14,20,22-tetren-3-one(25279-67-8) Related Product Information