4223-43-2 Usage
Uses
Used in Pharmaceutical Industry:
17B-ACETOXY-6B-HYDROXY-TESTOSTERONE is used as a pharmaceutical compound for its testosterone derivative properties. As a controlled substance, it may have potential applications in the development of medications targeting hormonal imbalances or conditions related to testosterone levels.
Used in Sports and Performance Enhancement:
17B-ACETOXY-6B-HYDROXY-TESTOSTERONE, being a testosterone derivative, is used as a performance-enhancing substance in sports. It may be sought after by athletes looking to improve their physical performance, although its use as such is generally prohibited and considered doping.
Used in Research and Development:
In the field of research and development, 17B-ACETOXY-6B-HYDROXY-TESTOSTERONE serves as a valuable compound for studying the effects of testosterone and its derivatives on the human body. This can lead to the discovery of new treatments for various medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 4223-43-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,2 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4223-43:
(6*4)+(5*2)+(4*2)+(3*3)+(2*4)+(1*3)=62
62 % 10 = 2
So 4223-43-2 is a valid CAS Registry Number.
4223-43-2Relevant academic research and scientific papers
Synthesis of a novel class of steroidal tetrazolo[1,5-a]pyridines via intramolecular 1,3-dipolar cycloadditions
Gogoi, Junali,Bezbaruah, Pranjal,Saikia, Pallabi,Goswami, Jonalee,Gogoi, Pranjal,Boruah, Romesh Chandra
scheme or table, p. 1497 - 1500 (2012/03/27)
A facile synthesis of a novel class of steroidal A/B/D-ring annulated tetrazolo[1,5-a]pyridine derivatives has been accomplished via intramolecular 1,3-dipolar cycloaddition reaction of azide with nitrile in aprotic solvent. The synthesis of D-ring annulated tetrazolo[1,5-a]pyridine in alcohol showed incorporation of an alcohol molecule into the heterocyclic system.
A Simple Acid-Catalyzed Isomerization of &γ-Hydroxy Enones into &γ-Diones
Wijnberg, Joannes B. P. A.,Jongedijk, Gerard,Groot, Aede de
, p. 2650 - 2654 (2007/10/02)
The acid-catalyzed isomerization of γ-hydroxy α,β-unsaturated ketones into γ-diones can be performed in high yields by using hydrogen bromide in ether.The utility of this functional group transformation is illustrated by its application to the synthesis of key intermediates 12a and 12b for rearranged drimanes, in steroid functionalization, and in the total synthesis of (+/-)-7-hydroxycostal.
