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Warfarin

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Identification
Molecular formula
C19H16O4N
CAS number
81-81-2
IUPAC name
2-(dimethylamino)ethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate
State
State

Warfarin is typically found in a solid state at room temperature. Its appearance as a crystalline powder makes it easy to handle in laboratory and medical settings. It is generally stored in a dry environment to maintain its stability and efficacy.

Melting point (Celsius)
161.00
Melting point (Kelvin)
434.00
Boiling point (Celsius)
301.00
Boiling point (Kelvin)
574.00
General information
Molecular weight
308.33g/mol
Molar mass
308.3340g/mol
Density
1.3187g/cm3
Appearence

Warfarin is a white to off-white crystalline powder. It is usually odorless and has a very mild, characteristic scent. The powder is slightly soluble in water but more soluble in ethanol and methanol.

Comment on solubility

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

The solubility of 2-(dimethylamino)ethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate can be influenced by various factors, such as its molecular structure, polarity, and the nature of the solvent. A few key points to consider are:

  • Molecular Structure: The presence of both hydrophilic (amine and carboxylate groups) and hydrophobic (chromene and phenyl moieties) regions in the molecule adds complexity to its solubility profile.
  • Polarity: Compounds with higher polarity tend to dissolve better in polar solvents (like water), while those with lower polarity are more suited to non-polar solvents (like hexane).
  • Temperature: The solubility can be affected by temperature; typically, an increase in temperature enhances solubility due to increased molecular movement.
  • pH: The ionization state of the carboxylate group can change with pH, influencing solubility. For instance, in a more basic environment, the carboxylate may exist in its ionized form, increasing solubility.
  • Concentration: At higher concentrations, solubility may decrease due to saturation effects, which can lead to precipitation of the compound.

In summary, the solubility of 2-(dimethylamino)ethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate is a multifaceted aspect shaped by a wide range of chemical interactions. Understanding these factors can facilitate better formulation strategies for applications in various fields such as pharmaceuticals and materials science.

Interesting facts

Interesting Facts about 2-(Dimethylamino)ethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate

This compound, a member of the chromene family, boasts several intriguing characteristics that make it notable in the realm of organic chemistry. Here are some exciting aspects:

  • Structural Versatility: The compound exemplifies structural diversity owing to its chromene backbone, which is renowned for its ability to participate in a variety of chemical reactions, including electrophilic substitutions and photochemical transformations.
  • Biological Significance: Compounds related to chromenes are of significant interest in medicinal chemistry. They have been studied for various biological activities such as anti-inflammatory, antioxidant, and anticancer properties, making them potential candidates in drug development.
  • Fluorescent Properties: Many chromene derivatives, including this compound, exhibit fluorescence. This characteristic can be exploited in applications ranging from biological imaging to the development of fluorescent sensors, highlighting their versatility in research and industry.
  • Facilitation of Chemical Reactions: The presence of the dimethylamino group enhances the nucleophilicity of the compound, making it potentially more reactive and useful in synthetic organic chemistry.
  • Potential Applications: Due to its unique structure, the compound may find applications in areas such as materials science, particularly in the design of organic light-emitting diodes (OLEDs) and other optoelectronic materials.

As a fascinating intersection of various fields including medicinal chemistry, materials science, and fluorescence studies, 2-(dimethylamino)ethyl 3-methyl-4-oxo-2-phenyl-chromene-8-carboxylate showcases the importance of exploring unconventional compounds in the quest for innovative solutions.

Synonyms
SCHEMBL10709531
2-(dimethylamino)ethyl 3-methyl-4-oxo-2-phenylchromene-8-carboxylate