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2-(2-fluoroethoxy)naphthalene

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Identification
Molecular formula
C12H11FO
CAS number
118394-47-7
IUPAC name
2-(2-fluoroethoxy)naphthalene
State
State

At room temperature, 2-(2-fluoroethoxy)naphthalene is a liquid. It is often handled in this state under standard laboratory conditions.

Melting point (Celsius)
-4.00
Melting point (Kelvin)
269.15
Boiling point (Celsius)
270.70
Boiling point (Kelvin)
543.85
General information
Molecular weight
190.22g/mol
Molar mass
190.2160g/mol
Density
1.1823g/cm3
Appearence

2-(2-fluoroethoxy)naphthalene is a clear, colorless to pale yellow liquid. It is typically transparent, allowing easy observation of any potential impurities or changes in consistency. The liquid state is characteristic of many aromatic ether compounds.

Comment on solubility

Solubility of 2-(2-fluoroethoxy)naphthalene

2-(2-fluoroethoxy)naphthalene, a compound characterized by its aromatic structure and ether functional group, exhibits specific solubility characteristics that make it unique. Its solubility can be understood through several key points:

  • Polarity: The presence of the fluoroethoxy group contributes to the compound's overall polarity. This can affect how it interacts with solvents.
  • Solvent Selection: Generally, 2-(2-fluoroethoxy)naphthalene is more soluble in polar organic solvents such as ethanol and acetone, rather than in non-polar solvents.
  • Temperature Dependence: The solubility of this compound often increases with temperature, allowing for better dissolution in heated solvents.
  • Chemical Stability: Its relative stability in various solvents contributes to its consistent solubility behavior.

In summary, the solubility of 2-(2-fluoroethoxy)naphthalene is dictated by its polarity and the selection of solvent, with polar solvents being more effective for achieving dissolution. As a rule of thumb, remembering the principle of "like dissolves like" will guide researchers and chemists in their efforts to solubilize this aromatic compound effectively. Always consider the context in which this compound is used, as solubility plays a crucial role in its applications.

Interesting facts

Interesting Facts about 2-(2-Fluoroethoxy)naphthalene

2-(2-Fluoroethoxy)naphthalene is an intriguing compound with significant relevance in various fields, notably in medicinal chemistry and materials science. Here are some fascinating aspects of this compound:

  • Structural Significance: The compound features a naphthalene ring, which is a polycyclic aromatic hydrocarbon. This structure contributes to its electronic properties and potential applications in organic electronics.
  • Fluorine Atom: The presence of the fluorine atom is crucial. Fluorinated compounds often exhibit enhanced biological activity and stability, making them a focus in pharmaceutical development.
  • Solubility Profile: The ethoxy group enhances solubility in organic solvents, a property that is beneficial in synthesis and formulation processes.
  • Potential Applications: Due to its structure, 2-(2-fluoroethoxy)naphthalene may serve as a building block in the synthesis of functional materials, dyes, and pharmaceuticals.

As a chemistry student or a scientist, exploring the reactions and interactions of such compounds can be greatly insightful. Especially, the study of how subtle modifications in a compound's structure can impact its properties opens up a world of possibilities in designing new materials and drugs. As Nobel laureate Frances H. Arnold once said, “What the scientist seeks, he must create.” The charm of compounds like 2-(2-fluoroethoxy)naphthalene lies in their ability to inspire innovative discoveries!

Synonyms
2-(2-Fluoroethoxy)naphthalene
325-24-6
2-Fluoroethyl 2-naphthyl ether
2-Naphthyl 2-fluoroethyl ether
Ether, 2-fluoroethyl 2-naphthyl
2-Fluoroethyl beta-naphthyl ether
NAPHTHALENE, 2-(2-FLUOROETHOXY)-
BRN 3242270
DTXSID10186223
4-06-00-04258 (Beilstein Handbook Reference)
SCHEMBL12354082
DTXCID20108714