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Warfarin

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Identification
Molecular formula
C19H16O4
CAS number
81-81-2
IUPAC name
6-amino-3-(2-oxo-2-pyrrolidin-1-yl-ethyl)chromen-2-one
State
State
Warfarin is a solid at room temperature.
Melting point (Celsius)
160.00
Melting point (Kelvin)
433.15
Boiling point (Celsius)
390.00
Boiling point (Kelvin)
663.15
General information
Molecular weight
308.34g/mol
Molar mass
308.3360g/mol
Density
1.2700g/cm3
Appearence

Warfarin appears as a crystalline powder that is white to off-white in color.

Comment on solubility

Solubility of 6-amino-3-(2-oxo-2-pyrrolidin-1-yl-ethyl)chromen-2-one

The solubility of 6-amino-3-(2-oxo-2-pyrrolidin-1-yl-ethyl)chromen-2-one is influenced by various factors, and understanding these can provide important insights into its potential applications. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound may exhibit moderate solubility in polar organic solvents such as ethanol and dimethyl sulfoxide (DMSO) due to the presence of functional groups that can engage in hydrogen bonding.
  • Temperature Dependence: Solubility can often increase with temperature; thus, heating the solvent may enhance the dissolution of this compound.
  • pH Sensitivity: The solubility may vary with pH, particularly due to the amino group which can be protonated or deprotonated in different pH conditions, allowing for increased solubility in more acidic or basic environments.
  • Hydrophobic Interactions: The chromenone structure may grant some hydrophobic properties, potentially limiting its solubility in pure water, which is typical for many organic compounds.

Overall, while the exact solubility profile of 6-amino-3-(2-oxo-2-pyrrolidin-1-yl-ethyl)chromen-2-one requires empirical determination, these factors highlight the complexity of solubility and the importance of conducting thorough solubility assays in various solvents and conditions.

Interesting facts

Interesting Facts about 6-amino-3-(2-oxo-2-pyrrolidin-1-yl-ethyl)chromen-2-one

This fascinating compound is a member of the chromone family, which is known for its diverse range of biological activities. Often categorized as a flavonoid, it has garnered attention for its potential pharmacological properties. Here are some intriguing points worth noting:

  • Pharmacological Potential: Studies have suggested that compounds like this can exhibit anti-inflammatory, antioxidant, and even anticancer activities, making them promising candidates for drug development.
  • Structure-Activity Relationship: The unique structural features of this compound, particularly the 2-oxo-2-pyrrolidin-1-yl group, contribute significantly to its biological activity, emphasizing the importance of molecular structure in medicinal chemistry.
  • Versatile Synthesis: Chemists have developed various synthetic pathways to create this compound, often utilizing innovative methods that highlight the evolving techniques in organic synthesis.
  • Application in Research: This compound serves as a valuable tool in various research fields, including pharmacology and toxicology, allowing scientists to explore its mechanisms of action and therapeutic potential.

As a compound that bridges theoretical and applied chemistry, 6-amino-3-(2-oxo-2-pyrrolidin-1-yl-ethyl)chromen-2-one not only captivates researchers but also presents a myriad of opportunities for future investigations. As we delve deeper into its properties, this compound could unveil new avenues for therapeutic advancements.

Synonyms
18144-58-6
6-Amino-3-((1-pyrrolidinylcarbonyl)methyl)coumarin
COUMARIN, 6-AMINO-3-((1-PYRROLIDINYLCARBONYL)METHYL)-
DTXSID10171154
DTXCID4093645
6-amino-3-(2-oxo-2-pyrrolidin-1-ylethyl)chromen-2-one
6-Amino-3-(2-oxo-2-(pyrrolidin-1-yl)ethyl)-2H-chromen-2-one
6-Amino-3-[(pyrrolidin-1-ylcarbonyl)methyl]coumarin
6-amino-3-[2-oxo-2-(pyrrolidin-1-yl)ethyl]-2H-chromen-2-one