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3α-ol-6-oxo-5β-24-cholanoic acid methyl ester is a complex organic compound belonging to the class of steroids. It is derived from cholesterol and is characterized by a specific arrangement of functional groups, including a hydroxyl group (-ol) at the 3α position, a ketone (-oxo) at the 6 position, and a carboxylic acid group at the 24 position. The compound is further modified by the esterification of the carboxylic acid with methanol, resulting in a methyl ester group. This chemical modification can influence the compound's solubility and reactivity. It is often found in various biological samples and is used in research to study steroid metabolism and related pathways. The compound's structure and properties make it a significant molecule in the field of biochemistry and endocrinology.

2862-62-6

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2862-62-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2862-62-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,6 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2862-62:
(6*2)+(5*8)+(4*6)+(3*2)+(2*6)+(1*2)=96
96 % 10 = 6
So 2862-62-6 is a valid CAS Registry Number.

2862-62-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3α-ol-6-oxo-5β-24-cholanoic acid methyl ester

1.2 Other means of identification

Product number -
Other names methyl 3α-hydroxy-6-oxo-5β-cholanoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2862-62-6 SDS

2862-62-6Relevant academic research and scientific papers

Structural modifications of deoxycholic acid to obtain three known brassinosteroid analogues and full NMR spectroscopic characterization

Herrera, Heidy,Carvajal, Rodrigo,Olea, Andrés F.,Espinoza, Luis

, (2016)

An improved synthesis route for obtaining known brassinosteroid analogues, i.e., methyl 2α,3α-dihydroxy-6-oxo-5α-cholan-24-oate (11), methyl 3α-hydroxy-6-oxo-7-oxa-5α-cholan-24-oate (15) and methyl 3α-hydroxy-6-oxa-7-oxo-5α-cholan-24-oate (16), from hyodeoxycholic acid (4) maintaining the native side chain is described. In the alternative procedure, the di-oxidized product 6, obtained in the oxidation of methyl hyodeoxycholate 5, was converted almost quantitatively into the target monoketone 7 by stereoselective reduction with NaBH4 , increasing the overall yield of this synthetic route to 96.8%. The complete 1H- and 13C-NMR assignments for all compounds synthesized in this work have been made by 1D and 2D heteronuclear correlation gs-HSQC and gs-HMBC techniques. Thus, it was possible to update the spectroscopic information of 1H-NMR and to accomplish a complete assignment of all 13C-NMR signals for analogues 5-16, which were previously reported only in partial form.

A Facile Route to Ursodeoxycholic Acid Based on Stereocontrolled Conversion and Aggregation Behavior Research

Dou, Qian,Jiang, Zhongliang

, p. 588 - 594 (2016/02/14)

A facile route to ursodeoxycholic acid (UDCA) and its aggregation behavior in aqueous phase solution, which is rarely known, are reported. The starting material, hyodeoxycholic acid (HDCA), is a relatively less expensive material and more easily obtained compared with chenodeoxycholic acid (CDCA). A facile route was developed to synthesize UDCA from HDCA with a Shapiro reaction as the key step and in 26% overall yield. A new strategy using organosilane reagent considering its stability, nontoxicity, and abundance in nature was carried out for a more rapid route and higher yield. It was found that the critical micelle concentration value, which is a critical value for surfactants of bile salts, was influenced by the number of hydroxyl groups.

PURIFICATION PROCESS FOR CHENODEOXYCHOLIC ACID

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Page/Page column 13-14, (2008/06/13)

The present invention relates to a process for purifying chenodeoxycholic acid (3α,7α-dihydroxy-5β-cholic acid). In particular, the present invention relates to a process for purifying chenodeoxycholic acid from low grade of chenodeoxycholic acid mixture in swine bile solid, with high yield and purity.

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