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Flavokawain B

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Identification
Molecular formula
C19H21NO3
CAS number
341213-25-4
IUPAC name
2,3-dimethyl-6-(1-piperidylmethyl)chromen-4-one
State
State

Flavokawain B is in a solid state at room temperature.

Melting point (Celsius)
158.00
Melting point (Kelvin)
431.15
Boiling point (Celsius)
680.15
Boiling point (Kelvin)
953.15
General information
Molecular weight
324.38g/mol
Molar mass
324.4100g/mol
Density
1.1222g/cm3
Appearence

Flavokawain B appears as a pale yellow crystalline powder. It is typically a solid at room temperature and can have a shiny crystalline structure.

Comment on solubility

Solubility of 2,3-Dimethyl-6-(1-piperidylmethyl)chromen-4-one

The compound 2,3-dimethyl-6-(1-piperidylmethyl)chromen-4-one exhibits interesting solubility characteristics due to its unique structural features. Understanding solubility is crucial as it affects various applications in pharmacology, chemistry, and materials science.

Key Points on Solubility:

  • Polar vs. Nonpolar: The presence of piperidine in the structure introduces polar functional groups, which may enhance solubility in polar solvents such as water or ethanol.
  • Effect of Alkyl Groups: The dimethyl substituents can increase lipophilicity, suggesting better solubility in nonpolar organic solvents.
  • Overall Compatibility: The compound might show moderate solubility in a mixed solvent system, balancing both polar and nonpolar characteristics.

In summary, the solubility of 2,3-dimethyl-6-(1-piperidylmethyl)chromen-4-one is influenced by its structural components, leading to varying interactions with solvents. As quoted by many chemists, “the solubility of a compound often determines its practical applications.” Understanding these solubility traits can enhance further studies and applications in drug development and chemical formulations.

Interesting facts

Interesting Facts about 2,3-Dimethyl-6-(1-Piperidylmethyl)chromen-4-one

The compound 2,3-dimethyl-6-(1-piperidylmethyl)chromen-4-one is an intriguing member of the flavonoid family, notable for its unique structure and potential applications. Here are some fascinating insights:

  • Structural Highlights: This compound features a chromenone core, which is a 2-phenyl-1-benzopyran-4-one structure. The dimethyl groups at positions 2 and 3 enhance its stability and possibly its reactivity.
  • Piperidine Connection: The presence of a 1-piperidylmethyl substituent introduces potential bioactivity, as piperidine derivatives are often associated with various pharmacological effects.
  • Potential Biological Activity: Due to its structure, this compound may exhibit antioxidant and anti-inflammatory properties, making it a candidate for research in health-related applications.
  • Pathway to Innovation: Compounds like these are often synthesized in laboratories for drug development. Scientists may explore their effects on various biological pathways.

In the words of a renowned chemist, “The beauty of chemistry lies in its ability to transform simple molecules into complex structures with novel properties.”
This compound embodies that beauty and holds promise for future discoveries in medicinal chemistry.

As research continues, the exploration of 2,3-dimethyl-6-(1-piperidylmethyl)chromen-4-one could unveil new therapeutic roles, illustrating the critical nature of synthetic organic chemistry in advancing our understanding of complex biological systems.