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Naproxen

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Identification
Molecular formula
C14H14O3
CAS number
22204-53-1
IUPAC name
(E)-2-(1-naphthyl)hex-4-enoic acid
State
State

Naproxen is a solid at room temperature.

Melting point (Celsius)
152.00
Melting point (Kelvin)
425.15
Boiling point (Celsius)
240.00
Boiling point (Kelvin)
513.15
General information
Molecular weight
230.26g/mol
Molar mass
230.2600g/mol
Density
1.1340g/cm3
Appearence

Naproxen appears as a white or off-white crystalline powder.

Comment on solubility

Solubility of (E)-2-(1-naphthyl)hex-4-enoic acid

(E)-2-(1-naphthyl)hex-4-enoic acid, a compound belonging to the class of organic acids, exhibits intriguing solubility characteristics that are important for its applications and behavior in various solvents.

Generally, the solubility of this compound can be influenced by several factors:

  • Polarity of Solvent: This acid might dissolve better in polar solvents such as ethanol or methanol, while being less soluble in non-polar solvents due to its naphthalene moiety.
  • Temperature: An increase in temperature often enhances the solubility of organic compounds, potentially allowing (E)-2-(1-naphthyl)hex-4-enoic acid to attain higher solubility in certain solvents.
  • Acidity and Basicity: As a carboxylic acid, it may exhibit increased solubility in basic conditions through the formation of a carboxylate salt, which is generally more soluble than the neutral form.

Despite these influencing factors, it is crucial to note that the solubility may vary according to the structure and interactions between the solute and solvent. As with many organic compounds, the solvent's nature is vital in determining how well (E)-2-(1-naphthyl)hex-4-enoic acid can dissolve.

In practical applications, understanding this solubility behavior can lead to optimized use in chemical syntheses and reactions where solubility plays a critical role.

Interesting facts

Interesting Facts about (E)-2-(1-naphthyl)hex-4-enoic acid

(E)-2-(1-naphthyl)hex-4-enoic acid is a fascinating compound belonging to the class of unsaturated carboxylic acids. With its unique structure, it not only piques the interest of chemists but also offers a range of applications in various fields. Here are some intriguing highlights:

  • Structural Diversity: This compound features a hexenoic acid backbone, which includes a double bond that introduces geometric isomerism and opens the door to numerous derivatives and reactions.
  • Inspired by Nature: Compounds like (E)-2-(1-naphthyl)hex-4-enoic acid are often inspired by naturally occurring substances, making them relevant in the study of natural product synthesis and drug development.
  • Applications in Pharmaceuticals: Its structural features make it a valuable candidate in the synthesis of biologically active molecules, potentially leading to the development of new therapeutic agents.
  • Materials Science: The functionality of the compound allows it to be explored in the creation of novel materials and polymers with improved properties, crucial for advancements in technology.
  • Intriguing Reactivity: The presence of the double bond within the compound allows for a variety of chemical reactions, including addition and polymerization, which are pivotal in organic chemistry.

In summary, (E)-2-(1-naphthyl)hex-4-enoic acid serves as an exemplary symbol of how synthetic organic compounds can bridge the gap between structure and function, paving the way for innovation in both chemical research and practical applications.