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Fluoxetine

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Identification
Molecular formula
C17H18NO2
CAS number
54910-89-3
IUPAC name
2-(diethylamino)ethyl 9H-fluorene-9-carboxylate
State
State

At room temperature, fluoxetine is typically found as a solid.

Melting point (Celsius)
179.70
Melting point (Kelvin)
452.85
Boiling point (Celsius)
299.70
Boiling point (Kelvin)
572.85
General information
Molecular weight
309.41g/mol
Molar mass
309.4140g/mol
Density
2.3000g/cm3
Appearence

Fluoxetine typically appears as a white to off-white crystalline solid. It can be odorless or have a faint amine-like odor.

Comment on solubility

Solubility of 2-(diethylamino)ethyl 9H-fluorene-9-carboxylate

The solubility of 2-(diethylamino)ethyl 9H-fluorene-9-carboxylate can be influenced by several factors, especially considering its unique structure. This compound features both hydrophobic and hydrophilic components, which can affect its interaction with various solvents.

In terms of solubility characteristics, it is essential to consider:

  • Polarity: The presence of the diethylamino group can impart a degree of polarity, which may enhance solubility in polar solvents such as water, though the hydrophobic fluorene moiety could counteract this effect.
  • Solvent Compatibility: This compound is likely to demonstrate better solubility in organic solvents like ethanol, dimethyl sulfoxide (DMSO), and acetone, which are capable of solubilizing larger organic molecules.
  • Concentration Considerations: The solubility may also vary with concentration; lower concentrations may yield different solubility behaviors than higher concentrations.

In summary, the solubility of 2-(diethylamino)ethyl 9H-fluorene-9-carboxylate is a complex interplay of its chemical structure and the nature of the solvent used. Understanding these solubility dynamics is crucial for applications in pharmaceuticals and materials science.

Interesting facts

Interesting Facts about 2-(diethylamino)ethyl 9H-fluorene-9-carboxylate

2-(diethylamino)ethyl 9H-fluorene-9-carboxylate is a fascinating compound that has intrigued scientists for various reasons. Below are some noteworthy aspects of this chemical:

  • Fluorene Derivative: As a derivative of fluorene, this compound showcases the unique properties associated with polycyclic aromatic compounds. Fluorene itself is known for its *stable structure* and *significant photochemical properties*.
  • Applications in Synthesis: The compound serves as a key building block in organic synthesis, particularly in the creation of more complex molecules. Its diethylamino group can impart distinctive reactivity, making it a valuable reagent.
  • Biological Activity: Studies have shown that compounds related to 9H-fluorene-9-carboxylate can exhibit various biological activities, including potential *antitumor* effects. This opens avenues for research in medicinal chemistry.
  • Fluorescent Properties: The fluorene moiety contributes to the compound's ability to fluoresce under UV light, which can be useful in fluorescent labeling and detection in biochemical assays.
  • Safety Precautions: Like many organic compounds, it is essential to understand safety protocols when handling this compound, particularly concerning its potential reactivity and toxicity.

In conclusion, 2-(diethylamino)ethyl 9H-fluorene-9-carboxylate is not just an ordinary chemical; it holds *great potential* in synthetic chemistry and biological applications while providing a platform for further exploration in various fields of study.

Synonyms
Pavatrin
Pavatrine
Aminocarbofluorene
Carbofluorene amino ester
UNII-23AHS3XR5K
23AHS3XR5K
BRN 2594285
DTXCID40118572
dtxsid30196081
Pavatrineat
9H-Fluorene-9-carboxylic acid, 2-(diethylamino)ethyl ester
FLUORENE-9-CARBOXYLIC ACID, 2-(DIETHYLAMINO)ETHYL ESTER
Q27253734