Chlormadinone acetate

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Identification

Molecular formula
C23H29ClO4
CAS Number
302-22-7
IUPAC Name
17-acetyl-6-chloro-17-hydroxy-10,13,16-trimethyl-2,8,9,11,12,14,15,16-octahydro-1H-cyclopenta[a]phenanthren-3-one
Molecular Weight
405.94g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3000g/cm3
Synonyms
Pregna-4, 6-diene-3, 20-dione, 6-chloro-17- hydroxy-16-methyl-, (16R)-
Interesting facts

Interesting Facts about 17-acetyl-6-chloro-17-hydroxy-10,13,16-trimethyl-2,8,9,11,12,14,15,16-octahydro-1H-cyclopenta[a]phenanthren-3-one

This compound, which falls under the category of synthetic steroids, has garnered attention in various fields, including medicinal chemistry. Here are some compelling facts about it:

  • Synthetic Derivative: It is a synthetic derivative of natural steroid hormones, showcasing human ingenuity in modifying molecular structures for specific biological effects.
  • Potential Applications: This compound has potential applications in hormone replacement therapies, particularly in treating conditions related to hormonal imbalances.
  • Pharmacological Activity: Researchers are interested in its pharmacological activity—specifically how modifications to its structure can influence its interaction with steroid receptors.
  • Chirality and Stereoisomerism: The presence of multiple chiral centers in its structure presents fascinating challenges in stereochemistry, often impacting its biological activity and effectiveness.
  • Environmental Stability: Understanding how it behaves in various environmental conditions is crucial for assessing its suitability in therapeutics as well as potential ecological impacts.

Overall, the modification of the steroid nucleus in this compound reflects a deeper understanding of chemistry and biology, contributing to developments in pharmaceuticals and therapeutic strategies. This compound exemplifies the balance between chemical innovation and the drive for effective medical solutions.


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