51504-01-9

Basic information

• Product Name: 3β-acetoxy-22ξ,23ξ-epoxy-4'-phenyl-5α,8α-ergost-6-eno<5,8-a>1',2',4'-triazolidine-3',5'-dione
• CAS NO: 51504-01-9
• Molecular Weight: 629.84
• Mol File: 51504-01-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3β-acetoxy-22ξ,23ξ-epoxy-4'-phenyl-5α,8α-ergost-6-eno<5,8-a>1',2',4'-triazolidine-3',5'-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 3β-acetoxy-22ξ,23ξ-epoxy-4'-phenyl-5α,8α-ergost-6-eno<5,8-a>1',2',4'-triazolidine-3',5'-dione(51504-01-9)
• EPA Substance Registry System: 3β-acetoxy-22ξ,23ξ-epoxy-4'-phenyl-5α,8α-ergost-6-eno<5,8-a>1',2',4'-triazolidine-3',5'-dione(51504-01-9)

Safety Data

• Hazardous Substances Data: 51504-01-9(Hazardous Substances Data)

Upstream product

• 28421-56-9 3β-acetoxy-5α,8α-(4-phenyl-1,2,4-triazolidine-3,5-dione-1,2-diyl)ergosta-6,22-diene 
• 4233-33-4 4-Phenyl-1,2,4-triazolidine-3,5-dione 
• 1108-03-8 ergosterol acetate 

Relevant articles and documents

Side-Chain Modified Ergosterol and Stigmasterol Derivatives as Liver X Receptor Agonists

A series of stigmasterol and ergosterol derivatives, characterized by the presence of oxygenated functions at C-22 and/or C-23 positions, were designed as potential liver X receptor (LXR) agonists. The absolute configuration of the newly created chiral ce

SELECTIVE OXIDATION OF THE DOUBLE BONDS IN THE 4-PHENYL-1,2,4-TRIAZOLINE-3,5-DIONE DIELS-ALDER ADDUCT OF ERGOSTEROL ACETATE

Methods for oxidations at the 6(7)-and 22(23)-double bonds in the phenyltriazoline adduct of ergosterol acetate (I) are described.KMnO4 and OsO4 were found to react with the 6(7)-double bond to yield the 6,7-glycol and osmate ester, respectively.Other rea