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Warfarin Nicotinate

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Identification
Molecular formula
C25H20NO4
CAS number
129-06-6
IUPAC name
2-hydroxy-4-phenyl-8-(piperidin-1-ium-1-ylmethyl)chromen-7-one;pyridine-4-carboxylate
State
State

Warfarin Nicotinate is in a solid crystalline state at room temperature, often found in pharmaceutical and laboratory settings.

Melting point (Celsius)
159.00
Melting point (Kelvin)
432.15
Boiling point (Celsius)
298.00
Boiling point (Kelvin)
571.15
General information
Molecular weight
398.44g/mol
Molar mass
398.4440g/mol
Density
1.2400g/cm3
Appearence

Warfarin Nicotinate presents as a crystalline solid substance, typically observed in a white to off-white color.

Comment on solubility

Solubility of 2-hydroxy-4-phenyl-8-(piperidin-1-ium-1-ylmethyl)chromen-7-one; pyridine-4-carboxylate

The solubility of 2-hydroxy-4-phenyl-8-(piperidin-1-ium-1-ylmethyl)chromen-7-one; pyridine-4-carboxylate can be significantly influenced by various factors, including its ionic interactions, polar functional groups, and the overall chemical environment.

Here are some key points regarding its solubility:

  • Ionic Nature: The presence of the piperidin-1-ium group suggests a likely solubility in water due to ionic interactions, which can promote dissolution in polar solvents.
  • Hydroxyl Group: The 2-hydroxy functional group enhances interaction with water molecules, possibly further increasing solubility.
  • Phenyl Group: The 4-phenyl moiety is hydrophobic, which may impede solubility in polar solvents, creating a balance between hydrophobic and hydrophilic characteristics.
  • Impact of Solvent: Solubility can vary considerably between different media, indicating potential applicability in organic solvents as well as in aqueous solutions.

In summary, the solubility of this compound can be considered relatively favorable due to its ionic nature and the presence of polar functional groups, while the hydrophobic portions may limit solubility in highly polar substances. Each context of use should be evaluated to determine the most effective medium for dissolution.

Interesting facts

Interesting Facts about 2-Hydroxy-4-phenyl-8-(piperidin-1-ium-1-ylmethyl)chromen-7-one; Pyridine-4-carboxylate

This unique compound, known for its complex structure, has garnered attention in various fields of research, particularly in the realms of medicinal and organic chemistry. Here are some intriguing aspects of this compound:

  • Structural Diversity: The molecular framework contains a chromen-7-one core, which is notable for its biological activity. The incorporation of functional groups like the piperidin-1-ium-1-ylmethyl moiety increases the structural diversity, making it a potential candidate for various biochemical interactions.
  • Biological Potential: Compounds with similar structures exhibit a wide range of pharmaceutical properties. This includes activities such as anti-inflammatory, antibacterial, and even anticancer effects. The ability of this compound to interact with biological receptors may lead to novel therapeutic applications.
  • Base Catalysis: The presence of the pyridine-4-carboxylate component suggests potential catalytic properties, making it interesting for organic synthesis processes. Pyridines are known to serve as excellent bases in catalysis, which might be harnessed in developing efficient chemical reactions.
  • Research Significance: Interest in this compound has been heightened within academia, especially among researchers working on drug design and discovery. Its complex nature encourages studies into its synthesis, mechanistic pathways, and interaction profiles.
  • Chemical Synthesis: The synthetic routes to create such compounds often involve multi-step reactions, providing opportunities for chemists to explore innovative methodologies and potentially discover new reaction pathways or conditions.
  • Material Applications: Beyond pharmaceuticals, compounds of this nature can inspire development in materials science, particularly in designing new polymers or advanced materials due to their distinctive properties.

In summary, 2-hydroxy-4-phenyl-8-(piperidin-1-ium-1-ylmethyl)chromen-7-one; pyridine-4-carboxylate appears to hold promise not just in medicinal chemistry but also in materials engineering, providing a fascinating avenue for ongoing research and development.