16265-24-0 Usage
Uses
Used in Organic Synthesis:
3-Keto-7α,12α-dihydroxy-5α-cholanic Acid is used as an intermediate in the synthesis of various organic compounds. Its unique structure allows it to serve as a building block for the creation of complex molecules, which can be further modified for specific applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-Keto-7α,12α-dihydroxy-5α-cholanic Acid is used as a precursor for the development of drugs targeting various health conditions. Its structural properties make it a valuable compound in the synthesis of novel therapeutic agents.
Used in Chemical Research:
3-Keto-7α,12α-dihydroxy-5α-cholanic Acid is also used in chemical research to study the properties and reactivity of bile acid derivatives. This knowledge can be applied to develop new methods and techniques in organic chemistry, as well as to understand the biological roles of these compounds.
Used in Cholesterol Research:
Due to its structural similarity to cholesterol, 3-Keto-7α,12α-dihydroxy-5α-cholanic Acid can be used in research related to cholesterol metabolism and its role in various diseases. This can lead to the development of new treatments for conditions such as atherosclerosis and hypercholesterolemia.
Check Digit Verification of cas no
The CAS Registry Mumber 16265-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,6 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 16265-24:
(7*1)+(6*6)+(5*2)+(4*6)+(3*5)+(2*2)+(1*4)=100
100 % 10 = 0
So 16265-24-0 is a valid CAS Registry Number.
16265-24-0Relevant academic research and scientific papers
Potential bile acid metabolites. XXI. A new synthesis of allochenodeoxycholic and allocholic acids
Iida,Nishida,Chang,Niwa,Goto,Nambara
, p. 763 - 765 (2007/10/02)
A new method for the preparation of allochenodeoxycholic and allocholic acids is described. The key steps in the synthesis are 1) simultaneous oxidation-dehydrogenation reaction of 3α-hydroxy 5β-bile acid formyl esters with iodoxybenzene catalyzed by benzeneseleninic anhydride, 2) reductive allomerization at C-5 of the 1,4-dien-3-oxo bydroxy acids with lithium/liq. ammonia, and 3) subsequent reduction of the resulting 3-oxo 5α-compounds with K-Selectride.
