(3a,5b,7a)-23-carboxy-7-hydroxy-24-norcholan-3-yl b-D-glucopyranosiduronic acid

Base Information

• Chemical Name: (3a,5b,7a)-23-carboxy-7-hydroxy-24-norcholan-3-yl b-D-glucopyranosiduronic acid
• CAS No.: 58814-71-4
• Molecular Formula: C30H48O10
• Molecular Weight: 568.7
• Mol file: 58814-71-4.mol

Synonyms:(3a,5b,7a)-23-carboxy-7-hydroxy-24-norcholan-3-yl b-D-glucopyranosiduronic acid;(3a,5b,7a)-23-carboxy-7-hydroxy-24-norcholan-3-yl-b-D-Glucopyranosiduronic acid

Chemical Property of (3a,5b,7a)-23-carboxy-7-hydroxy-24-norcholan-3-yl b-D-glucopyranosiduronic acid

Chemical Property:

• Vapor Pressure: 1.1E-26mmHg at 25°C
• Refractive Index: 1.593
• Boiling Point: 760.3°Cat760mmHg
• PKA: 2.82±0.70(Predicted)
• Flash Point: 242.9°C
• Density: 1.34g/cm³
• Storage Temp.: Hygroscopic, Refrigerator, under inert atmosphere
• Solubility.: DMSO (Slightly), Methanol (Slightly), Water (Slightly)

Purity/Quality:

99%min ^*data from raw suppliers

ChenodeoxycholicAcid-3-β-D-glucuronide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Uses: Chenodeoxycholic acid-3-β-D-glucuronide is a derivative of chenodeoxycholic acid (C291900). Chenodeoxycholic acid is a major bile acid in many vertebrates, occurring as the N-glycine and/or N-taurine conjugate. With other bile acids, forms mixed micelles with lecithin in bile which solubilize cholesterol and thus facilitates its excretion. Fcilitates fat absorption in the small intestine by micellar solubilization of fatty acids and monoglycerides. Anticholelithogenic. Epimeric with Ursodiol.

Technology Process of (3a,5b,7a)-23-carboxy-7-hydroxy-24-norcholan-3-yl b-D-glucopyranosiduronic acid

There total 1 articles about (3a,5b,7a)-23-carboxy-7-hydroxy-24-norcholan-3-yl b-D-glucopyranosiduronic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ (2S,3S,4S,5R,6R)-6-[(3R,5R,7R,8R,9S,10S,13R,14S,17R)-17-(3-Carboxy-1-methyl-propyl)-7-hydroxy-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthren-3-yloxy]-3,4,5-trihydroxy-tetrahydro-pyran-2-carboxylic acid (58814-71-4,129121-77-3)

Guidance literature:

Diester IVa, NaOH;