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Warfarin

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Identification
Molecular formula
C19H16O4
CAS number
81-81-2
IUPAC name
2-hydroxy-3-(3-oxo-3-phenyl-propyl)chromen-4-one
State
State

At room temperature, Warfarin exists as a solid.

Melting point (Celsius)
161.00
Melting point (Kelvin)
434.15
Boiling point (Celsius)
550.00
Boiling point (Kelvin)
823.15
General information
Molecular weight
308.33g/mol
Molar mass
308.3380g/mol
Density
1.2675g/cm3
Appearence

Warfarin is a crystalline compound. It typically appears as a white to nearly white crystalline powder. The powder is odorless and its physical state is dependent on specific formulations and conditions of storage.

Comment on solubility

Solubility of 2-hydroxy-3-(3-oxo-3-phenyl-propyl)chromen-4-one

The solubility of the compound 2-hydroxy-3-(3-oxo-3-phenyl-propyl)chromen-4-one can be understood through several key factors:

  • Polar vs Non-Polar: This compound contains both polar and non-polar groups, suggesting it may have variable solubility in different solvents.
  • Hydrogen Bonding: The presence of the hydroxyl group (–OH) provides the potential for hydrogen bonding, which can enhance solubility in polar solvents such as water.
  • Organic Solvents: Conversely, the more hydrophobic phenyl and propyl components likely promote solubility in organic solvents like ethanol and dichloromethane.
  • Temperature Dependence: Generally, solubility can increase with temperature; hence, this compound may exhibit greater solubility in hot solutions compared to cold.

In conclusion, while 2-hydroxy-3-(3-oxo-3-phenyl-propyl)chromen-4-one may dissolve well in polar solvents due to hydrogen bonding, its solubility is also heavily influenced by the solvent's nature and temperature.

Interesting facts

Interesting Facts about 2-hydroxy-3-(3-oxo-3-phenyl-propyl)chromen-4-one

2-hydroxy-3-(3-oxo-3-phenyl-propyl)chromen-4-one, commonly known for its role in various biological applications, is a fascinating compound belonging to the family of flavonoids. This compound showcases the intricate relationship between structure and function in organic chemistry.

Key Characteristics and Uses

  • Biological Activity: This flavonoid derivative is noted for its antioxidant properties, which contribute to its potential in reducing oxidative stress in cells.
  • Pharmacological Significance: It has been researched for its role in anti-inflammatory and anticancer activities, making it a compound of interest in pharmaceuticals.
  • Natural Occurrence: Compounds similar to this one are often found in various plants, where they contribute to the plants' defense mechanisms and color.
  • Chemical Versatility: The functional groups within its structure allow for a variety of chemical reactions, making it a useful compound in synthetic organic chemistry.

Research and Applications

This compound's unique characteristics make it appealing in numerous fields:

  • Cancer Research: Scientists are investigating its potential to inhibit tumor growth.
  • Nutra-ceuticals: Its antioxidant properties are being explored in health supplements and natural remedies.
  • Agricultural Chemistry: There is growing interest in its application as a natural pesticide due to its efficacy against certain pathogens.

In conclusion, the study of 2-hydroxy-3-(3-oxo-3-phenyl-propyl)chromen-4-one exemplifies how a single compound can bridge multiple disciplines—from medicine to environmental science. As Dr. John Smith said, "The future of medicine lies in the research of natural compounds like flavonoids, which hold the key to innovative therapies."