82341-96-6 Usage
Chemical structure
A synthetic chemical compound derived from testosterone, containing a 19-iodo group, a 3beta-hydroxy group, a 17-one carbonyl group, and an acetate ester.
Classification
A powerful steroid with potential anabolic and androgenic effects.
Research and laboratory use
Often used in research and laboratory settings to study its effects on muscle growth and development.
Potential applications
Fields of medicine, pharmacology, and performance enhancement.
Hormone replacement therapy
Studied for its potential use in hormone replacement therapy.
Effects on muscle growth
Investigated for its impact on muscle growth and development.
Legal status
The legal status of 19-IODO-5-ANDROSTENE-3BETA-OL-17-ONE 3-ACETATE may vary depending on the country or region, as it may be classified as a controlled substance or have restrictions on its use.
Dosage and administration
Dosage and administration guidelines should be followed carefully, as misuse can lead to adverse effects.
Availability
Availability may be limited to research or laboratory settings, and obtaining the compound may require specific permissions or licenses.
Please note that this information is provided for educational purposes only and should not be considered medical advice. Always consult with a healthcare professional before using any new substances or treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 82341-96-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,4 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 82341-96:
(7*8)+(6*2)+(5*3)+(4*4)+(3*1)+(2*9)+(1*6)=126
126 % 10 = 6
So 82341-96-6 is a valid CAS Registry Number.
82341-96-6Relevant academic research and scientific papers
Ito,Ogawa,Maeda,Kojima
, p. 131 - 144 (1983)
19-Iodinated and 6 beta-iodomethyl-19-nor derivatives of cholesterol and 17-ketosteroid labeled with 131I were tested in rats to determine the critical structural features required for maximal adrenal uptake. The introduction of the 17-keto group in place of the 17 beta-side chain of cholesterol caused most of the radioactivity to be taken up by the thyroids. Fluorination at the C-3 position had deleterious effects on the adrenal concentration and led to the loss of adrenal specificity. A beta-hydroxy group at the C-3 position is substantially required for adrenal uptake.
