24643-97-8 Usage
Description
Indenestrol, also known as Indenestrol-d3, is an impurity that is formed during the synthesis of isotope-labelled metabolites of Diethylstibestrol (D445026). It is a chemical compound with a unique structure that has potential applications in various fields due to its specific properties.
Uses
Used in Pharmaceutical Industry:
Indenestrol is used as an impurity in the synthesis of isotope-labelled metabolites for pharmaceutical research and development. Its presence in the synthesis process is crucial for the production of these metabolites, which can be used for various applications, such as studying the metabolism and pharmacokinetics of Diethylstibestrol.
Used in Research and Development:
Indenestrol is used as a research compound for studying the properties and behavior of Diethylstibestrol and its metabolites. This can help scientists understand the mechanisms of action, potential side effects, and therapeutic applications of Diethylstibestrol, leading to the development of more effective drugs and treatments.
Used in Quality Control and Analysis:
Indenestrol can be used as a reference compound in quality control and analysis of pharmaceutical products containing Diethylstibestrol or its metabolites. By comparing the properties and behavior of the test samples with the known characteristics of Indenestrol, researchers and quality control professionals can ensure the purity, potency, and safety of the pharmaceutical products.
Check Digit Verification of cas no
The CAS Registry Mumber 24643-97-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,4 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 24643-97:
(7*2)+(6*4)+(5*6)+(4*4)+(3*3)+(2*9)+(1*7)=118
118 % 10 = 8
So 24643-97-8 is a valid CAS Registry Number.
InChI:InChI=1/C18H18O2/c1-3-15-16-9-8-14(20)10-17(16)11(2)18(15)12-4-6-13(19)7-5-12/h4-11,19-20H,3H2,1-2H3
24643-97-8Relevant articles and documents
Effects of (+)-, (-)- and (±)-indenestrols A and B on microtubule polymerization
Oda,Sakakibara,Sato,Hanzawa,Hata
, p. 588 - 592 (2007/10/02)
Indenestrol A (IA) is a metabolite of diethylstilbestrol (DES), and indenestrol B (IB) is an analog of IA. IA was simply obtained from E,E-dienestrol in the presence of dilute sulfuric acid, and a mixture of IA and IB was formed by thermal cyclization of
