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Warfarin

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

At room temperature, Warfarin is in a solid state, typically as a crystalline powder.

Melting point (Celsius)
161.00
Melting point (Kelvin)
434.15
Boiling point (Celsius)
760.00
Boiling point (Kelvin)
1 033.15
General information
Molecular weight
308.34g/mol
Molar mass
308.3350g/mol
Density
1.2430g/cm3
Appearence

Warfarin appears as a white to almost white crystalline powder. It is typically odorless and may appear in a polymorphic form, but generally maintains a consistent crystalline structure.

Comment on solubility

Solubility of 2-(diethylamino)ethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate

The solubility of 2-(diethylamino)ethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate can be characterized by several key factors:

  • Polarity: As a compound featuring both a diethylamino group and a chromene structure, it exhibits a balance of polar and non-polar characteristics. Compounds with such structural features often show varied solubility in different solvents.
  • Solvent Interaction: Typically, it is more soluble in organic solvents like ethanol, methanol, and dimethyl sulfoxide (DMSO), owing to the hydrophobic nature of the phenyl and chromene moieties.
  • Aqueous Solubility: Because of its amphiphilic nature, the solubility in water may be limited, particularly at lower temperatures. However, factors such as pH and the presence of other ions can affect its solubility in aqueous environments.
  • Temperature Influence: As with many organic compounds, solubility tends to increase with temperature, which can be significant for applications needing dissolvability in higher concentrations.

In summary, the solubility of 2-(diethylamino)ethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate is notably influenced by solvent type, temperature, and molecular interactions, making it a compound of interest for various applications in chemical and biological fields.

Interesting facts

Exploring 2-(Diethylamino)ethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate

The compound 2-(diethylamino)ethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate is an intriguing molecule, combining several functional groups that contribute to its distinctive properties and potential applications. As a member of the chromene family, this compound incorporates a fused chromene ring structure that plays a vital role in its reactivity and interactions. Here are several key points about this fascinating compound:

  • Pharmacological Potential: Due to its structural features, compounds of this type are often investigated for their biological activity, particularly in medicinal chemistry, where they may demonstrate anti-inflammatory or anti-cancer properties.
  • Diverse Applications: The presence of the diethylamino group can enhance solubility and bioavailability, making it a candidate for formulations in pharmaceutical research.
  • Synthetic Versatility: The preparation of this compound allows for modifications at various positions, potentially yielding new derivatives with tailored characteristics for specific applications.
  • Role in Organic Electronics: Some derivatives of chromenes are explored in organic electronic devices due to their photophysical properties, such as luminescence.

Furthermore, the complexity of its structure invites scientists to delve into various interdisciplinary studies, encompassing organic synthesis, material science, and pharmacology. It’s a perfect example of how a single compound can bridge gaps across multiple fields of research.

In conclusion, 2-(diethylamino)ethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate exemplifies the beauty and utility of organic compounds, reminding us that chemistry plays a crucial role in advancing technology and medicine.