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| | 5 alpha-stigmastane-3 beta,5,6 beta-triol 3-monobenzoate Basic information |
| Product Name: | 5 alpha-stigmastane-3 beta,5,6 beta-triol 3-monobenzoate | | Synonyms: | 5 alpha-stigmastane-3 beta,5,6 beta-triol 3-monobenzoate;Stigmastane-3,5,6-triol;Stigmastane-3beta,5alpha,6beta-triol;Stigmastane-3,5,6-triol, (3β,5α,6β)-;5α;6β-triol;Stigmastane-3β;Stigmastane-3β,5α,6β-triol | | CAS: | 20835-91-0 | | MF: | C29H52O3 | | MW: | 448.72 | | EINECS: | | | Product Categories: | | | Mol File: | 20835-91-0.mol |  |
| | 5 alpha-stigmastane-3 beta,5,6 beta-triol 3-monobenzoate Chemical Properties |
| Melting point | 224-226.5 °C | | Boiling point | 535.6±40.0 °C(Predicted) | | density | 1.047±0.06 g/cm3(Predicted) | | solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | | form | Powder | | pka | 14.26±0.70(Predicted) |
| | 5 alpha-stigmastane-3 beta,5,6 beta-triol 3-monobenzoate Usage And Synthesis |
| Uses | Sitostanetriol (Sitostane-3β,5α,6β-triol) is a steroid isolated from Casearia membranacea (Flacourtiaceae)[1]. | | Definition | ChEBI: A 3beta-hydroxy steroid that is stigmastane substituted by hydroxy groups at positions 3, 5 and 6 (the 3beta,5alpha,6beta stereoisomer). It has been isolated from the roots of Brey
ia fruticosa. | | target | Antifection | | References | [1] Chang KC, et al. A cytotoxic butenolide, two new dolabellane diterpenoids, a chroman and a benzoquinol derivative formosan Casearia membranacea. Planta Med. 2003 Jul;69(7):667-72. DOI:10.1055/s-2003-41120 |
| | 5 alpha-stigmastane-3 beta,5,6 beta-triol 3-monobenzoate Preparation Products And Raw materials |
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