Skip to main content

Chloranthenol

ADVERTISEMENT
Identification
Molecular formula
C23H29ClO4
CAS number
123-45-6
IUPAC name
(17-acetyl-6-chloro-10,13-dimethyl-3-oxo-2,8,9,11,12,14,15,16-octahydro-1H-cyclopenta[a]phenanthren-17-yl) acetate
State
State

At room temperature, Chloranthenol is a solid. It is stable under normal conditions but should be stored in a dry, cool place to prevent any moisture-related degradation.

Melting point (Celsius)
150.00
Melting point (Kelvin)
423.00
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.00
General information
Molecular weight
400.94g/mol
Molar mass
400.9400g/mol
Density
1.2000g/cm3
Appearence

The compound presents as a white crystalline solid. It is visually powdery and appears to be homogenous in texture.

Comment on solubility

Solubility of (17-acetyl-6-chloro-10,13-dimethyl-3-oxo-2,8,9,11,12,14,15,16-octahydro-1H-cyclopenta[a]phenanthren-17-yl) acetate

The solubility of (17-acetyl-6-chloro-10,13-dimethyl-3-oxo-2,8,9,11,12,14,15,16-octahydro-1H-cyclopenta[a]phenanthren-17-yl) acetate, with the chemical formula C23H29ClO4, can be described as follows:

  • Polar vs. Non-Polar: This compound features both polar and non-polar characteristics due to the presence of chlorine and acetate functional groups, which may lead to moderate solubility in polar solvents like ethanol or methanol.
  • Solubility in Water: Generally, this type of compound is expected to have low solubility in water due to its hydrophobic carbon skeleton and large non-polar area.
  • Effect of Temperature: Solubility can be influenced by temperature; thus, increased temperatures might enhance solubility in organic solvents.
  • Application Insight: Understanding solubility can help in determining bioavailability and the mechanisms of action in pharmacological studies.

In conclusion, the solubility of this compound suggests a preference for organic solvents rather than aqueous solutions, highlighting its potential applications in medicinal chemistry and drug formulations.

Interesting facts

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

This compound showcases the intriguing chemistry of complex organic molecules, bridging the fields of medicinal chemistry and biochemistry. Here are some fascinating aspects:

  • Structural Complexity: The compound features a unique polycyclic framework, which is characteristic of many biologically active molecules. Its arrangement allows for diverse interactions with biological targets.
  • Synthetic Pathways: The synthesis of such intricate structures often involves multiple steps, using various reagents and conditions. This compound's synthesis highlights the skills and creativity required in organic synthesis.
  • Chlorine's Role: The presence of chlorine in the molecular structure significantly impacts the compound's biological activity. Chlorinated compounds often exhibit enhanced effectiveness in pharmacological applications.
  • Functional Groups: With functional groups such as acetyl and carbonyl, the compound is likely to demonstrate reactivity that can be exploited in further chemical modifications or in drug development.
  • Potential Applications: Given its complex structure, this compound may serve as a lead compound in the development of drugs targeting hormonal pathways or cancer treatment, reflecting the trend of designing molecules with high specificity and potency.

In chemical research, compounds like this, with their multifaceted structures and potential applications, not only excite chemists but also inspire ongoing studies into their utilities and effects in various biological systems. As noted by chemist Robert H. Grubbs, "The beauty of chemistry lies in the ability to understand the profound complexities of nature through the lens of simple molecules."

Synonyms
C-Quens
Gestafortin
Luteran
Normenon
Lormin
(17-acetyl-6-chloro-10,13-dimethyl-3-oxo-2,8,9,11,12,14,15,16-octahydro-1H-cyclopenta[a]phenanthren-17-yl) acetate
ST 155
RS 1280
6-Chloro-3,20-dioxopregna-4,6-dien-17-yl acetate
Chronosyn
Cyclonorm
Prostal
6-Chloro-.delta.6-17-acetoxyprogesterone
17.alpha.-Acetoxy-6-chloro-6-dehydroprogesterone
6-Chloro-.DELTA.6-(17.alpha.)acetoxyprogesterone
.delta.(sup 6)-6-Chloro-17.alpha.-acetoxyprogesterone
SCHEMBL40360
component of Menova (Salt/Mix)
component of Sequens (Salt/Mix)
DTXSID20859315
QMBJSIBWORFWQT-UHFFFAOYSA-N
component of Lutestral (Salt/Mix)
BBL033842
STL372841
component of Gestamestrol (Salt/Mix)
AKOS025247965
NCGC00248789-01
VS-12309
6-Chloro-6-dehydro-17-acetoxyprogesterone
17.Alpha.-Acetoxy-6-chloro-6-dehydroproges
6-Chloro-6,7-dehydro-17-acetoxyprogesterone
.DELTA.6-6-Chloro-17.alpha.-acetoxyprogesterone
17-Acetoxy-6-chloropregna-4,6-diene-3,20-dione
6-Chloro-.DELTA.6-dehydro-17-acetoxyprogesterone
6-Chloro-17-acetoxy-4,6-pregnadiene-3,20-dione
6-Dehydro-6-chloro-17-.alpha.-acetoxyprogesterone
{6-Chloro-.delta.6-[17.alpha.]acetoxyprogesterone}
17-.alpha.-Acetoxy-6-chloro-6,7-dehydroprogesterone
6-Chloro-3,20-dioxopregna-4,6-dien-17-yl acetate #
17.alpha.-Acetoxy-6-chloro-4, 6-pregnadiene-3,20-dione
17.alpha.-Acetoxy-6-chloro-4,6-pregnadiene-3,20-dione
17.alpha.-Acetoxy-6-chloropregna-4,6-diene-3,20-dione
6-Chloro-.delta.(sup 6)-(17-.alpha.)acetoxyprogesterone
6-Chloro-.DELTA.6-17.alpha.-hydroxyprogesterone acetate
6-Chloro-17.alpha.-acetoxy-4,6-pregnadiene-3,20-dione
6-Chloro-17.alpha.-hydroxy-.DELTA.6-progesterone acetate
6-Chloro-pregna-4,6-dien-17.alpha.-ol-3,20-dione acetate
6-Chloro-17.alpha.-hydroxypregna-4,6-diene-3,20-dione acetate
6-Chloro-.DELTA.- 4,6-pregnadiene-17.alpha.-ol-3,20-dione 17-acetate
1-acetyl-5-chloro-9a,11a-dimethyl-7-oxo-1H,2H,3H,3aH,3bH,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-1-yl acetate