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12-Oxo-5β-cholan-24-oic acid methyl ester is a chemical compound derived from the bile acid family, specifically a derivative of cholic acid. It is characterized by the presence of a ketone group at the 12th carbon position and a carboxylic acid group at the 24th carbon position. The compound is further modified by the esterification of the carboxylic acid group with a methyl group, resulting in a methyl ester. This modification can influence the compound's solubility and reactivity. In the context of its chemical structure, it is important to note that the 5β-cholan refers to the stereochemistry at the 5th carbon, which is in the β-configuration. 12-Oxo-5β-cholan-24-oic acid methyl ester is of interest in the field of organic chemistry and may have applications in the synthesis of pharmaceuticals or as an intermediate in the preparation of other complex organic molecules.

1173-30-4

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1173-30-4 Usage

Chemical structure

Steroidal compound with a methyl ester group attached to the carboxylic acid moiety.

Bile acid derivative

Derived from lithocholic acid, a naturally occurring bile acid.

Function in digestion

Involved in the emulsification of fats and absorption of lipids in the small intestine.

Signaling molecule

Regulates various physiological processes, including lipid metabolism, glucose homeostasis, and inflammation.

Therapeutic applications

Studied for potential use in treating metabolic disorders, liver diseases, and gastrointestinal conditions.

Cancer research

Investigated for its role in cancer prevention and treatment.

Biological functions

Plays a crucial role in various biological functions and has potential implications for human health.
These properties and specific content provide a comprehensive overview of the characteristics and potential applications of 12-Oxo-5β-cholan-24-oic acid methyl ester.

Check Digit Verification of cas no

The CAS Registry Mumber 1173-30-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,7 and 3 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1173-30:
(6*1)+(5*1)+(4*7)+(3*3)+(2*3)+(1*0)=54
54 % 10 = 4
So 1173-30-4 is a valid CAS Registry Number.

1173-30-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 12-keto-5β-cholan-24-oic acid methyl ester

1.2 Other means of identification

Product number -
Other names 12-Oxo-5β-cholansaeure-methylester

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:1173-30-4 SDS

1173-30-4Relevant academic research and scientific papers

Improved enantioselectivity in the epoxidation of cinnamic acid derivatives with dioxiranes from keto bile acids

Bortolini, Olga,Fantin, Giancarlo,Fogagnolo, Marco,Forlani, Roberto,Maietti, Silvia,Pedrini, Paola

, p. 5802 - 5806 (2007/10/03)

The asymmetric epoxidation of substituted cinnamic acids has been obtained in the presence of different keto bile acid derivatives as optically active carbonyl inducers and Oxone as oxygen source. Predominant or almost exclusive formation of both enantiomeric epoxides is obtained (ee up to 95%) depending on the specific substitution at carbons C(7) and C(12) of the bile acid.

Autooxidation of Cholanic Acid in the Presence of Ferrous Ions

Sawaya, Takuji,Kimura, Michiya

, p. 1207 - 1212 (2007/10/02)

Autooxidation of cholanic acid in an aqueous acetone solution containing 0.2 M acetate buffer (pH 5.0) and ferrous sulfate gave three C(12)-keto products, A, B, and C.The main product A was elucidated to be 12-oxo-5β-cholan-24-oic acid.The minor product B

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