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3α-Acetoxy-7,12-dioxo-5β-cholan-24-oic acid methyl ester is a complex organic compound belonging to the class of bile acids. It is characterized by a cholestane skeleton, which is a steroid nucleus with a cyclopentane ring fused to a phenanthrene nucleus. The compound features a 3α-acetoxy group, indicating an acetate ester at the 3α position, and a 5β-cholan structure, which means the hydroxyl group at the 5 position is oriented in the β-configuration. Additionally, it has two carbonyl groups at the 7 and 12 positions, and a carboxylic acid group at the 24 position, which is esterified with a methyl group. 3α-Acetoxy-7,12-dioxo-5β-cholan-24-oic acid methyl ester is a derivative of cholic acid, a naturally occurring bile acid that plays a crucial role in the digestion and absorption of fats. The methyl ester group suggests that it is a synthetic modification of the parent bile acid, potentially altering its solubility or reactivity.

7753-73-3

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7753-73-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7753-73-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,5 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7753-73:
(6*7)+(5*7)+(4*5)+(3*3)+(2*7)+(1*3)=123
123 % 10 = 3
So 7753-73-3 is a valid CAS Registry Number.

7753-73-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3α-acetyloxy-7,12-dioxo-5β-cholan-24-oate

1.2 Other means of identification

Product number -
Other names methyl 3α-acetoxy-7,12-dioxo-5β-cholan-24-oate

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:7753-73-3 SDS

7753-73-3Relevant academic research and scientific papers

Differentially-protected steroidal triamines; scaffolds with potential for medicinal, supramolecular, and combinatorial chemistry

Amo, Vicente Del,Siracusa, Laura,Markidis, Theodoros,Baragana, Beatriz,Bhattarai, Khadga M.,Galobardes, Marta,Naredo, Gregorio,Perez-Payan, M. Nieves,Davis, Anthony P.

, p. 3320 - 3328 (2007/10/03)

Cholic acid 2a has been converted into two new orthogonally-protected triamino scaffolds, 13 and 14. The synthesis proceeds via the bis-Boc-NH-substituted azide 10, for which an improved preparation is described. After removal of the Boc groups, the two a

The 'triamino-analogue' of methyl cholate; a practical, large-scale synthesis

Davis, Anthony P.,Pérez-Payán, M. Nieves

, p. 991 - 993 (2007/10/03)

The triamino steroids 2 are in demand as facial amphiphiles and starting materials for supramolecular chemistry. 2 (R = Me)is now available from cholic acid 1 in substantial quantities via a new, high-yielding procedure.

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