6808-14-6

Basic information

• Product Name: (25R)-Furosta-5,20(22)-diene-3β,26-diol
• Synonyms: (25R)-Furosta-5,20(22)-diene-3β,26-diol;Pseudodiosgenin
• CAS NO: 6808-14-6
• Molecular Formula: C₂₇H₄₂O₃
• Molecular Weight: 414.62058
• Mol File: 6808-14-6.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (25R)-Furosta-5,20(22)-diene-3β,26-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (25R)-Furosta-5,20(22)-diene-3β,26-diol(6808-14-6)
• EPA Substance Registry System: (25R)-Furosta-5,20(22)-diene-3β,26-diol(6808-14-6)

Safety Data

• Hazardous Substances Data: 6808-14-6(Hazardous Substances Data)

Usage

General Description

(25R)-Furosta-5,20(22)-diene-3β,26-diol is a steroidal compound with a furostane skeleton. It is a type of sapogenin, which is a natural steroid precursor found in various plants. This chemical has potential medicinal properties and is being studied for its potential use in pharmaceuticals. It has been associated with a range of biological activities including anti-inflammatory, immunomodulatory, and anticancer effects. Additionally, it has been investigated for its potential to lower cholesterol levels and improve cardiovascular health. Overall, (25R)-Furosta-5,20(22)-diene-3β,26-diol is a promising compound with potential therapeutic applications.

Upstream product

• 512-04-9 diosgenin 
• 64-17-5 ethanol 
• 65682-56-6 (25R)-furosta-5,16,20(22)-triene-3β,26-diol 
• 141-78-6 ethyl acetate 
• 2309-38-8 pseudodiosgenin diacetate 
• 470-05-3 (3β,20R,22R,25R)-spirosol-5-en-3-ol 
• 122190-71-0 (25R)-3β-acetoxy-26-benzoyloxy-furosta-5,20(22)-diene 
• 122273-19-2 (25R)-3β-acetoxy-26-butyryloxy-furosta-5,20(22)-diene 
• 7604-96-8 C₂₉H₄₄O₄ 

Downstream Products

• 1573153-97-5 C₄₁H₅₄O₇S₂ 
• 991-62-8 (3b,25R)-3-hydroxyfurosta-5,20⁽²²⁾-dien-26-yl 4-Methylbenzenesulfonate 
• 55028-76-7 (3β,20S,22S,25R)-22-thiospirosol-5-en-3-ol 
• 93176-77-3 3,26-dimethoxy-23-(p-dimethylaminobenzylidenyl)-furost-5,20-diene 
• 512-04-9 diosgenin 
• 470-05-3 (3β,20R,22R,25R)-spirosol-5-en-3-ol 

Relevant articles and documents

Synthesis and cytotoxic effect of pseudodiosgenyl saponins with thio-ring F

Both the sugar moieties and aglycons of steroid saponins play important roles for their bioactivities. In order to test the biological contribution of the glycosyl residue and search new saponins with notable anticancer activity, mono- and di-saccharide p

KHSO4-SiO2-MeOH An efficient selective solid-supported system for deprotection of alcohols from esters

KHSO4-SiO2 can efficiently deprotect alcohols from esters through transesterification in methanol under mild condition. Esters of aromatic alcohols are easily transesterified at room temperature compared to the corresponding aliphatic or alicyclic alcohol. NAcetyl compounds and ethers are resistant to the reagent under the above condition. The method is very useful for preparation of biodiesel methyl ricinoleate from castor oil.

Studies on the coloration mechanism of furostanol derivatives with Ehrlich reagents. I. On the reaction of 3,26-dimethoxy-furost-5,20-diene with Ehrlich reagent

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