3,5-Cycloergosta-6,8(14),22-triene | CAS:24352-51-0

Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

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Prev Nutr Food Sci.2024, 29(4):504-511.

J Nat Med.2021, doi: 10.1007.

Appl. Sci. 2021, 11(22), 10552

Plants (Basel).2021, 10(12):2795.

Rec. Nat. Prod.2024, 18:4,405-418.

Plant J.2017, 90(3):535-546

Food Sci Nutr.2019, 8(1):246-256

J of l. Chroma.&Related Tech2020, 43(11-12):414-423.

Separations2023, 10(4), 231.

Microchemical Journal2024, 200:110475

Journal of the American Chemical Society, 1952, 74(21):469-74.

An i-Steroid Hydrocarbon from Ergosterol1.[Reference: WebLink]

METHODS AND RESULTS:
Reinvestigation of a hydrocarbon resulting from dehydration of ergosterol with either phosphorus oxychloride or p-toluenesulfonyl chloride in pyridine and heretofore regarded as an ergostatetraene has shown that the substance is 3,5-cyclo-Δ6, 8(14), 22-ergostatriene (3,5-Cycloergosta-6,8(14),22-triene, V), the first known i-steroid in the ergosterol series. Reaction of the hydrocarbon with hydrogen chloride and its acid-catalyzed hydration result in opening of the cyclopropane ring with formation of mixtures of ergosteryl chlorides or of ergosterol isomers; ergosterol-B1 of reasonable purity has been isolated from the product of hydration. A hydrocarbon, first described by Windaus, resulting from acid-catalyzed dehydration of 3α- and 3β-hydroxy-Δ4,7,22-ergostatriene was investigated to see if it corresponded to a highly dextrorotatory, alumina-isomerized impurity accompanying the i-steroid V.
CONCLUSIONS:
The results indicate that the Windaus hydrocarbon is Δ4,6,8(14),22-ergostatetraene (XIV). Formulas attributed earlier to hydrocarbons resulting from dehydration of epialloergosterol (NaOAc-Ac2O, see III) and of lumisterol (C10-epimer of III) are consistent with present evidence. "Ergosterol-E" is shown to consist largely of a mixture of dihydroergosterols.

Product Name	3,5-Cycloergosta-6,8(14),22-triene
CAS No.:	24352-51-0
Catalog No.:	CFN98257
Molecular Formula:	C₂₈H₄₂
Molecular Weight:	378.6 g/mol
Purity:	>=98%
Type of Compound:	Steroids
Physical Desc.:	Powder
Source:	From Poria cocos(Schw.)Wolf
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price: