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Methyl 3-[3-(2-fluoroethylamino)phenyl]propanoate

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Identification
Molecular formula
C12H16FNO2
CAS number
1279027-63-1
IUPAC name
methyl 3-[3-(2-fluoroethylamino)phenyl]propanoate
State
State

At room temperature, this compound is primarily in a liquid state. It should be stored in a cool, dry place, away from sources of ignition and direct sunlight.

Melting point (Celsius)
36.50
Melting point (Kelvin)
309.65
Boiling point (Celsius)
326.90
Boiling point (Kelvin)
600.05
General information
Molecular weight
253.26g/mol
Molar mass
253.2880g/mol
Density
1.2242g/cm3
Appearence

Methyl 3-[3-(2-fluoroethylamino)phenyl]propanoate typically appears as a colorless to light yellow liquid, depending on its purity. It has a distinctive chemical odor associated with esters and aromatic amines.

Comment on solubility

Solubility of Methyl 3-[3-(2-fluoroethylamino)phenyl]propanoate

Methyl 3-[3-(2-fluoroethylamino)phenyl]propanoate, a complex organic compound, exhibits varying solubility characteristics that are influenced by its unique molecular structure.

Factors Influencing Solubility

Here are some key factors to consider when evaluating the solubility of this compound:

  • Polarity: The presence of both polar and non-polar groups in the molecule affects its overall solubility profile. Typically, compounds with polar functional groups tend to dissolve better in polar solvents.
  • Hydrogen Bonding: The ability of the compound to form hydrogen bonds can enhance solubility in certain solvents, particularly water.
  • Temperature: Increasing temperature generally increases solubility, particularly for organic compounds, as heat allows for greater molecular movement.

Solubility in Different Solvents

This compound is likely to show:

  • In Water: Moderate solubility due to the presence of polar functional groups, though it may not be highly soluble.
  • In Organic Solvents: Increased solubility is anticipated in organic solvents such as ethanol or acetone, where its non-polar characteristics can be better accommodated.

As a general guideline, “the solubility of a compound reflects the compatibility between the solute and solvent at the molecular level.” Hence, understanding the solubility behavior of methyl 3-[3-(2-fluoroethylamino)phenyl]propanoate can be crucial for its applications in various chemical processes and formulations.

Interesting facts

Overview of Methyl 3-[3-(2-fluoroethylamino)phenyl]propanoate

Methyl 3-[3-(2-fluoroethylamino)phenyl]propanoate is a fascinating compound due to its unique structure and potential applications in various fields. This compound has attracted attention in medicinal chemistry and drug development. Here are some interesting facts:

Unique Structural Features

  • Fluorine Substitution: The presence of a fluorine atom in the ethylamino group enhances the compound's biological activity and lipophilicity, making it an appealing candidate for pharmacological studies.
  • Phenyl Ring: The incorporation of a phenyl group can lead to interesting interactions within biological systems, often influencing the compound's binding affinity to targets.
  • Esters: As an ester, this compound may participate in various organic reactions, potentially serving as a building block for more complex compounds.

Potential Applications

  • Drug Development: Methyl 3-[3-(2-fluoroethylamino)phenyl]propanoate may have implications in the synthesis of new pharmaceuticals, especially in areas targeting neurological or psychological conditions.
  • Agricultural Chemistry: The compound's unique properties might also lead to applications in agrochemicals, possibly contributing to the development of more effective herbicides or insecticides.
  • Research Tools: It could also serve as a useful tool in chemical biology, assisting in exploring protein interactions or enzyme activity.

Quote from the Field

As a chemist studying the impacts of molecular structure on biological activity, one often notes that, "Small changes in molecular composition can lead to significant shifts in pharmacological profiles." This compound epitomizes that principle.

In conclusion, Methyl 3-[3-(2-fluoroethylamino)phenyl]propanoate stands out with its intriguing chemistry and potential applications. Its unique structural features and versatile nature make it a compound worthy of further study in the realms of drug discovery and chemical synthesis.

Synonyms
S7GNC8TS3A
Methyl 3-[(2-fluoroethyl)amino]benzenepropanoate
Z6918824899
Benzenepropanoic acid, 3-[(2-fluoroethyl)amino]-, methyl ester
737690-98-1