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9-Fluorononan-2-one

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Identification
Molecular formula
C9H17FO
CAS number
407-82-1
IUPAC name
9-fluorononan-2-one
State
State
At room temperature, 9-fluorononan-2-one is in a liquid state. It is largely stable in ambient conditions but should be handled carefully due to its volatility and potential for skin and respiratory irritation.
Melting point (Celsius)
-99.00
Melting point (Kelvin)
174.15
Boiling point (Celsius)
223.20
Boiling point (Kelvin)
496.35
General information
Molecular weight
160.22g/mol
Molar mass
160.2170g/mol
Density
1.0031g/cm3
Appearence

9-Fluorononan-2-one is typically a clear to pale yellow liquid. It has a slightly oily texture and a sharp, pungent odor often associated with ketones and organofluorines. The liquid is viscous and flows relatively slowly compared to less dense liquids.

Comment on solubility

Solubility of 9-fluorononan-2-one

9-fluorononan-2-one, with its distinctive chemical structure, exhibits unique solubility characteristics that can be influenced by various factors. Below are some insights into its solubility:

  • Polarity: Due to the presence of the carbonyl group (C=O) and the fluorine atom, 9-fluorononan-2-one demonstrates a degree of polarity. This affects its solubility in different solvents.
  • Solvent Compatibility: In general, 9-fluorononan-2-one is expected to be soluble in organic solvents such as:
    • Alcohols
    • Aromatic hydrocarbons
    • Dichloromethane
  • Water Solubility: Since 9-fluorononan-2-one has a relatively long hydrocarbon chain, its solubility in water is likely to be low. This is typical for organic compounds with larger alkyl groups.
  • Temperature Effects: The solubility of such compounds often increases with temperature, as warmer conditions can help overcome solvation barriers.

In essence, while 9-fluorononan-2-one may dissolve readily in non-polar and mildly polar solvents due to its hydrophobic nature, its interaction with water is minimal, making it a fascinating compound to consider in various chemical applications. As always, experimentation is key to understanding the complete solubility profile of this intriguing molecule.

Interesting facts

Exploring 9-Fluorononan-2-one

9-Fluorononan-2-one is an intriguing compound that belongs to the class of ketones, characterized by the presence of a carbonyl group within its molecular structure. This compound has garnered interest not only for its chemical properties but also for its potential applications in various fields of research.

Interesting Facts:

  • Fluorination: The introduction of the fluorine atom at the 9-position is significant, as fluorinated compounds are often more stable and have unique reactivity patterns compared to their non-fluorinated counterparts. This makes them valuable in pharmaceuticals and agrochemicals.
  • Synthetic Utility: 9-Fluorononan-2-one serves as a versatile intermediate for the synthesis of more complex organic molecules, particularly in the fields of drug development and material science.
  • Biological Activity: Compounds like 9-fluorononan-2-one can exhibit interesting biological activities, making them useful in testing for anti-inflammatory or anti-cancer properties.
  • Chirality: The presence of a carbonyl group can influence the chirality of the compound, which is critical in determining the behavior of molecules in biological systems.

A quote emphasizing the importance of fluorinated compounds is: "Fluorine is a game changer in organic chemistry; it alters reactivity, stability, and even biological activity."

Overall, 9-fluorononan-2-one exemplifies how the manipulation of simple structures can lead to profound implications in modern chemistry and beyond.

Synonyms
9-Fluoro-2-nonanone
2-NONANONE, 9-FLUORO-
BRN 1752581
DTXSID60202785
4-01-00-03354 (Beilstein Handbook Reference)
DTXCID90125276
9-fluorononan-2-one
544-43-4