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| | 3,5-Dihydroxyergosta-7,22-dien-6-one Basic information |
| Product Name: | 3,5-Dihydroxyergosta-7,22-dien-6-one | | Synonyms: | 5alpha-Ergosta-7,22-diene-3beta,5beta-diol-6-one;6-Dehydrocerevisterol;(22E,24R)-3beta,5alpha-dihydroxyergosta-7,22-dien-6-one;3,5-Dihydroxyergosta-7,22-dien-6-one;Ergosta-7,22-dien-6-one, 3,5-dihydroxy-, (3β,5α,22E)-;3β,5α-Dihydroxyergosta-7,22-dien-6-one;5-Dihydroxyergosta-7;22-dien-6-one | | CAS: | 14858-07-2 | | MF: | C28H44O3 | | MW: | 428.65 | | EINECS: | | | Product Categories: | | | Mol File: | 14858-07-2.mol |  |
| | 3,5-Dihydroxyergosta-7,22-dien-6-one Chemical Properties |
| Melting point | 250 °C | | Boiling point | 550.569±50.00 °C(Press: 760.00 Torr)(predicted) | | density | 1.084±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted) | | solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | | form | Powder | | pka | 12.346±0.70(predicted) |
| | 3,5-Dihydroxyergosta-7,22-dien-6-one Usage And Synthesis |
| Uses | 6-Dehydrocerevisterol is a Steroids product that can be isolated from the fruit body of Ganoderma lucidum[1]. | | Definition | ChEBI: An ergostanoid that is (22E)-ergosta-7,22-diene substituted by hydroxy groups at position 3 and 5 and an oxo group at position 6 (the 3beta,5alpha stereoisomer). It has been isolated from Aspergillu
ochraceus. |
| | 3,5-Dihydroxyergosta-7,22-dien-6-one Preparation Products And Raw materials |
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