20835-91-0 Usage
Description
5 alpha-stigmastane-3 beta,5,6 beta-triol 3-monobenzoate is a 3beta-hydroxy steroid that is stigmastane substituted by hydroxy groups at positions 3, 5, and 6 (the 3beta,5alpha,6beta stereoisomer). It is a naturally occurring compound that has been isolated from the roots of Breynia fruticosa, a plant species.
Uses
Used in Pharmaceutical Industry:
5 alpha-stigmastane-3 beta,5,6 beta-triol 3-monobenzoate is used as a pharmaceutical compound for its potential therapeutic applications. The expression is: 5 alpha-stigmastane-3 beta,5,6 beta-triol 3-monobenzoate is used as a pharmaceutical compound for its potential therapeutic applications.
Used in Cosmetic Industry:
5 alpha-stigmastane-3 beta,5,6 beta-triol 3-monobenzoate is used as an ingredient in the cosmetic industry for its potential benefits in skincare products. The expression is: 5 alpha-stigmastane-3 beta,5,6 beta-triol 3-monobenzoate is used as an ingredient in the cosmetic industry for its potential benefits in skincare products.
Used in Research and Development:
5 alpha-stigmastane-3 beta,5,6 beta-triol 3-monobenzoate is used as a research compound for studying its chemical properties, biological activities, and potential applications in various fields. The expression is: 5 alpha-stigmastane-3 beta,5,6 beta-triol 3-monobenzoate is used as a research compound for studying its chemical properties, biological activities, and potential applications in various fields.
Please note that the provided materials do not specify any particular application for 5 alpha-stigmastane-3 beta,5,6 beta-triol 3-monobenzoate. The uses mentioned above are general applications based on the compound's properties and potential in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 20835-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,3 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 20835-91:
(7*2)+(6*0)+(5*8)+(4*3)+(3*5)+(2*9)+(1*1)=100
100 % 10 = 0
So 20835-91-0 is a valid CAS Registry Number.
InChI:InChI=1/C29H52O3/c1-7-20(18(2)3)9-8-19(4)23-10-11-24-22-16-26(31)29(32)17-21(30)12-15-28(29,6)25(22)13-14-27(23,24)5/h18-26,30-32H,7-17H2,1-6H3/t19-,20-,21+,22+,23-,24+,25+,26-,27-,28-,29+/m1/s1
20835-91-0Relevant articles and documents
Efficient trans-diaxial hydroxylation of Δ5-steroids
Carvalho, Jo?o F.S.,Silva, M. Manuel Cruz,Sá e Melo, M. Luisa
experimental part, p. 2455 - 2462 (2010/06/14)
A convenient, fast, and high-yielding process to synthesize 5α,6β-dihydroxysteroids directly from the correspondent Δ5-steroids is reported. The reaction protocol consists in the conjugation of a readily available and stable oxidant, magnesium bis(monoperoxyphthalate) hexahydrate, with the non-toxic bismuth(III) triflate in acetone to afford the trans-diaxial hydroxylation product in a stepwise manner and in excellent yields.
Gram-scale chromatographic purification of β-sitosterol: Synthesis and characterization of β-sitosterol oxides
Zhang, Xin,Geoffroy, Philippe,Miesch, Michel,Julien-David, Diane,Raul, Francis,Aoude-Werner, Dalal,Marchioni, Eric
, p. 886 - 895 (2007/10/03)
An effective purification method for β-sitosterol was developed starting from a commercial source of a phytosterol mixture using preparative adsorption column chromatography. β-Sitosterol (≥95% purity) was obtained on a gram-scale. Thus, the synthesis of six β-sitosterol oxides, including 7α-hydroxy, 7β-hydroxy, 5,6α-epoxy, 5,6β-epoxy, 7-keto, and 5α,6β-dihydroxysitosterol, were successfully carried out. The spectral characteristics of all the synthetic intermediates and target compounds (～95% purity) were well-documented.
Biological evaluation in vivo and in vitro of selected 5-alpha-cholestane-3-beta, 5-alpha, 6-beta-triol analogs as hypocholesterolemic agents.
Witiak,Parker,Brann,Dempsey,Ritter,Connor,Brahmankar
, p. 216 - 222 (2007/10/14)
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