7753-72-2 Usage
Uses
Used in Research Applications:
5BETA-CHOLANIC ACID 3,7-DIONE METHYL ESTER is used as a research chemical for the investigation of its properties and potential applications in various scientific fields. Its structural relationship with steroid hormones makes it a valuable compound for studying the mechanisms of hormone action and related biological processes.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, 5BETA-CHOLANIC ACID 3,7-DIONE METHYL ESTER serves as a precursor in the synthesis of other biologically active molecules. Its role in the creation of new drugs is significant, as it can contribute to the development of medications targeting a range of health conditions.
Used in Gastrointestinal and Hepatic Disorder Treatment:
Due to its relationship with bile acids, 5BETA-CHOLANIC ACID 3,7-DIONE METHYL ESTER may have therapeutic properties that are beneficial in the treatment of gastrointestinal and hepatic disorders. Its potential use in this area is based on the understanding of bile acids' role in digestion and liver function, suggesting that this compound could be instrumental in managing or treating related health issues.
Check Digit Verification of cas no
The CAS Registry Mumber 7753-72-2 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 7753-72:
(6*7)+(5*7)+(4*5)+(3*3)+(2*7)+(1*2)=122
122 % 10 = 2
So 7753-72-2 is a valid CAS Registry Number.
7753-72-2Relevant articles and documents
DEUTERATED BILE ACIDS
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Paragraph 0051, (2015/04/28)
This disclosure relates to deuterated bile acid compositions. A deuterated compound is selected from the disclosed groups of bile acids and their derivatives, analogs and salts. At least one of the hydrogen atoms in the compound is replaced with deuterium.
Selective dimethyldioxirane oxidation of bile acid methyl esters
Buxton, P. Christopher,Marples, Brian A.,Toon, Richard C.,Waddington, Victoria L.
, p. 4729 - 4732 (2007/10/03)
DMDO oxidation of the hydroxy groups of bile acid methyl esters establishes the positional order of reactivity as 3-7 > 6 > 12 and supports a mechanism involving C-H oxygen insertion through a planar intramolecularly hydrogen bonded transition state.
BILE ACIDS LXIX. SELECTIVE K-SELECTRIDE REDUCTION OF 3,7-DIKETO STEROIDS
Tal, Daniel M.,Frisch, G. Douglas,Elliott, William H.
, p. 851 - 854 (2007/10/02)
The K-Selectride reduction at low temperature (-45 C) of 7-oxo-5α-cholestan-3β-yl acetate and methyl 7-oxo-3α-hydroxy-5β-cholanoate resulted in almost quantitative yield of the 7α-alcohol in the 5α-compound but only moderate yield of the 5β-analog.The simultaneous reduction of two carbonyl in the 3 and 7 positions afforded good to excellent yields of the diaxial diol in planar steroids (methyl 3,7-dioxo-5α-cholanoate, 3,7-dioxo-5α-cholestane and methyl 3,7-dioxo-5α-cholestan-27-oate) and only 14percent of 3α,7α-(OH)2 from methyl 3,7-dioxo-5β-cholanoate.
