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Flavone

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Identification
Molecular formula
C23H23NO2
CAS number
17576-65-1
IUPAC name
3-methyl-2-phenyl-6-(1-piperidylmethyl)chromen-4-one
State
State

At room temperature, this compound is typically found in a solid crystalline form.

Melting point (Celsius)
178.00
Melting point (Kelvin)
451.00
Boiling point (Celsius)
450.00
Boiling point (Kelvin)
723.00
General information
Molecular weight
353.47g/mol
Molar mass
353.4650g/mol
Density
1.2160g/cm3
Appearence

The compound typically appears as a crystalline solid.

Comment on solubility

Solubility of 3-methyl-2-phenyl-6-(1-piperidylmethyl)chromen-4-one

3-methyl-2-phenyl-6-(1-piperidylmethyl)chromen-4-one, a member of the chromenone family, exhibits notable solubility characteristics which can be influenced by several factors:

  • Solvent Polarity: The solubility of this compound in various solvents is largely dictated by the polarity of the solvent used. Non-polar solvents may not dissolve the compound effectively due to its hydrophobic regions.
  • pH Sensitivity: The solubility can change with pH, especially if the compound contains functional groups that are ionizable. This phenomenon is particularly crucial in biological and pharmaceutical contexts.
  • Temperature Effects: Increased temperatures often enhance solubility. For 3-methyl-2-phenyl-6-(1-piperidylmethyl)chromen-4-one, higher temperatures may facilitate dissolution, thereby increasing its bioavailability.
  • Hydrogen Bonding: The presence of functional groups that can form hydrogen bonds may increase solubility in polar solvents like water, which is critical for potential medicinal applications.

In summary, the solubility of 3-methyl-2-phenyl-6-(1-piperidylmethyl)chromen-4-one is multifaceted, relying on solvent choice, pH, temperature, and molecular interactions. Understanding these factors can enable better utilization of the compound in various applications, particularly in the pharmaceutical industry.

Interesting facts

Interesting Facts about 3-methyl-2-phenyl-6-(1-piperidylmethyl)chromen-4-one

The compound 3-methyl-2-phenyl-6-(1-piperidylmethyl)chromen-4-one belongs to a class of organic compounds known as chromones. These compounds are derivatives of flavones and have garnered significant interest in various fields of research.

Key Highlights:

  • Pharmaceutical Potential: Compounds like this one often exhibit diverse biological activities. Some chromones have been studied for their anti-inflammatory, antioxidant, and antimicrobial properties, making them potential candidates for drug development.
  • Structural Diversity: The unique structure, characterized by the fusion of a chromone and a piperidine ring, provides an attractive framework for further chemical modifications. This structural versatility is crucial for enhancing pharmacological activity.
  • Natural Occurrences: Chromone derivatives can be found in various plants, contributing to their medicinal properties. The study of these compounds in nature can provide insights into their chemical ecology and potential health benefits for humans.
  • Research Applications: Synthetic studies involving this compound may focus on establishing its mechanism of action. Understanding how such compounds interact at the molecular level could reveal important information about disease pathways.

In summary, 3-methyl-2-phenyl-6-(1-piperidylmethyl)chromen-4-one is a fascinating compound that exemplifies the intersection of chemistry and biology, with potential implications in medicinal chemistry and therapeutic applications. Its study continues to inspire chemists and biologists alike, often leading to exciting discoveries that expand our knowledge of chemical compounds.