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Warfarin

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Identification
Molecular formula
C19H16O4
CAS number
81-81-2
IUPAC name
2-morpholinoethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate
State
State

At room temperature, warfarin is typically in a solid crystalline state.

Melting point (Celsius)
160.00
Melting point (Kelvin)
433.15
Boiling point (Celsius)
422.30
Boiling point (Kelvin)
695.45
General information
Molecular weight
308.34g/mol
Molar mass
308.3350g/mol
Density
1.2130g/cm3
Appearence

Warfarin is a white to off-white, crystalline powder. It is odorless and has a slightly bitter taste.

Comment on solubility

Solubility of 2-morpholinoethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate

The solubility of 2-morpholinoethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate can be characterized by a few important factors:

  • Solvent Compatibility: This compound is primarily soluble in organic solvents such as ethanol, dimethyl sulfoxide (DMSO), and dimethylformamide (DMF) due to its aromatic character and polar functional groups.
  • Temperature Influence: Increased temperatures often enhance solubility in organic solvents, which may facilitate its dissolution in practical applications.
  • pH Sensitivity: The solubility may also fluctuate with pH levels, affecting the ionization state of the carboxylate functional group.

It is essential to consider that “like dissolves like,” meaning that the polarity of the solvent should ideally match that of the compound for optimal solubility. Consequently, testing various solvents and conditions can yield precise solubility data, which is critical for applications in synthesis and drug formulation. Understanding these solubility traits allows for better predictions in its reactivity and applicability in chemical processes.

Interesting facts

Interesting Facts About 2-Morpholinoethyl 3-Methyl-4-Oxo-2-Phenyl-Chromene-8-Carboxylate

This compound, 2-morpholinoethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate, is a fascinating example of a chromene derivative. Chromenes are an important class of compounds in organic chemistry, deriving much of their significance from their diverse biological activities and potential therapeutic uses.

Key Characteristics

  • Biological Activity: Chromene derivatives, including this one, have been studied for their potential as anti-inflammatory, antioxidant, and anticancer agents.
  • Structural Complexity: The presence of a morpholino group contributes to the molecule's solubility and biological functionality, allowing it to penetrate cell membranes more easily.
  • Synthetic Interest: The synthesis of chromene-based compounds often involves intricate organic reactions, revealing a layer of complexity that can be both challenging and rewarding for chemists.

Applications

Research has indicated that compounds similar to this one may show promise in various fields:

  • Pharmaceutical Industry: Their potential role as drug candidates continues to be explored due to their ability to interact with biological targets.
  • Material Science: Some chromene derivatives have applications in creating pigments and dyes, showcasing their versatility beyond medicinal chemistry.

As a student or researcher in chemistry, understanding the implications of such complex structures can deepen your appreciation for molecular design and its potential contributions to science. When examining this compound, it's crucial to consider not just its molecular structure, but also the myriad of reactions it might participate in and the potential it holds for future studies in medicinal chemistry. Remember, in the words of a great chemist, "The magic of chemistry lies in the connections we make, not just the compounds we create."

Synonyms
SCHEMBL10707910