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Fluoro-MADAM

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Identification
Molecular formula
C23H25FN2O2
CAS number
1354631-79-4
IUPAC name
1-(4-fluorophenyl)-4-(9-methoxy-2,4,5,6-tetrahydro-1H-azepino[4,5-b]indol-3-yl)butan-1-one
State
State
Fluoro-MADAM is generally found in a solid state at room temperature, appearing as a powder that may clump together depending on environmental conditions such as humidity.
Melting point (Celsius)
148.50
Melting point (Kelvin)
421.65
Boiling point (Celsius)
523.95
Boiling point (Kelvin)
797.10
General information
Molecular weight
370.44g/mol
Molar mass
370.4420g/mol
Density
1.2900g/cm3
Appearence

Fluoro-MADAM typically appears as an off-white solid powder. Its appearance can vary slightly based on purity and preparation methods, but it is generally a crystalline powder with no significant odor.

Comment on solubility

Solubility of 1-(4-fluorophenyl)-4-(9-methoxy-2,4,5,6-tetrahydro-1H-azepino[4,5-b]indol-3-yl)butan-1-one

The solubility of 1-(4-fluorophenyl)-4-(9-methoxy-2,4,5,6-tetrahydro-1H-azepino[4,5-b]indol-3-yl)butan-1-one can be analyzed considering several factors that influence the dissolution behavior of this compound.

Factors Affecting Solubility

Some key factors affecting the solubility include:

  • Polarity: The presence of polar functional groups can enhance solubility in polar solvents.
  • Molecular Weight: Generally, lower molecular weight compounds tend to be more soluble.
  • Hydrogen Bonding: Capable of forming hydrogen bonds can increase solubility in water.
  • Temperature: Increasing temperature often enhances solubility for solid solutes.

Solvent Compatibility

This compound is likely to demonstrate variable solubility based upon the solvent:

  • Polar solvents: May improve solubility due to the presence of polar functional groups.
  • Nonpolar solvents: Limited solubility can be expected as nonpolar environments may not interact favorably with polar features.

In general, the unique structure of 1-(4-fluorophenyl)-4-(9-methoxy-2,4,5,6-tetrahydro-1H-azepino[4,5-b]indol-3-yl)butan-1-one suggests that its solubility might be more pronounced in organic solvents compared to aqueous environments. Understanding its solubility characteristics is crucial for its applications in various fields, particularly in pharmaceuticals and chemical synthesis.

Interesting facts

Interesting Facts about 1-(4-Fluorophenyl)-4-(9-methoxy-2,4,5,6-tetrahydro-1H-azepino[4,5-b]indol-3-yl)butan-1-one

This compound is a fascinating member of the class of compounds known as ketones, specifically featuring an intricate structure that includes a substituted aromatic ring and a cyclic amine. Here are some engaging insights about this compound:

  • Structural Diversity: The molecule showcases a unique combination of features, including a 4-fluorophenyl group and a tetrahydro-1H-azepino unit. This structural complexity is indicative of its potential for diverse biological activities.
  • Pharmacological Interest: Compounds with such structures often exhibit interesting pharmacological properties. The presence of both a ketone and an azepine could imply various mechanisms of action, holding promise for use in medicinal chemistry.
  • Synthetic Challenges: The synthesis of this compound can pose significant challenges due to its complexity, requiring multi-step procedures that ensure selectivity and yield. Researchers often employ advanced synthetic strategies to construct such intricate molecules.
  • Fluorination Impact: The inclusion of a fluorine atom in the phenyl ring can enhance the compound's metabolic stability and bioavailability. This alteration in structure could significantly affect how the compound interacts within biological systems.
  • Exploration in Drug Development: Given its intricate structure and potential biological relevance, this compound may serve as a starting point for the development of new therapeutic agents aimed at treating various diseases.

Overall, 1-(4-fluorophenyl)-4-(9-methoxy-2,4,5,6-tetrahydro-1H-azepino[4,5-b]indol-3-yl)butan-1-one epitomizes the intersection of synthetic chemistry and pharmacology, highlighting the importance of exploring novel compounds in the quest for innovative therapeutics.