9-Fluoro-1-phenyl-nonan-1-one | Solubility of Things

Identification

Molecular formula

C₁₅H₁₉FO

CAS number

IUPAC name

9-fluoro-1-phenyl-nonan-1-one

State

This compound is a liquid at room temperature, indicating higher volatility than typical solids. Its appearance as a clear, colorless liquid is indicative of many ketones with a moderate hydrocarbon and aromatic content.

Melting point (Celsius)

-45.00

Melting point (Kelvin)

228.15

Boiling point (Celsius)

260.00

Boiling point (Kelvin)

533.15

General information

Molecular weight

236.32g/mol

Molar mass

236.3190g/mol

Density

1.0159g/cm³

Appearence

9-Fluoro-1-phenyl-nonan-1-one is typically a clear colorless liquid. It may have a characteristic aromatic odor typically associated with ketones containing a phenyl group.

Comment on solubility

Solubility of 9-fluoro-1-phenyl-nonan-1-one

9-fluoro-1-phenyl-nonan-1-one, with its complex structure, showcases unique solubility characteristics. Understanding its solubility can provide insights into its behavior in various environments. Here are some key points to consider:

Solvent Polarity: The solubility of 9-fluoro-1-phenyl-nonan-1-one is largely influenced by the polarity of the solvent used. It tends to dissolve well in non-polar or slightly polar solvents due to its hydrophobic characteristics.
Temperature Influence: Higher temperatures generally increase the solubility of organic compounds. Thus, heating the solvent may improve the dissolution of this compound.
pH Dependencies: Although this compound does not possess acidic or basic functionalities, environmental pH may still subtly affect its solubility in specific contexts.
Chain Length Effect: The long nonane chain contributes to its non-polar traits, which may limit solubility in polar solvents like water but enhance solubility in organic solvents.

In summary, while 9-fluoro-1-phenyl-nonan-1-one does not exhibit simple solubility behavior, recognizing the impact of solvent choice and temperature can assist in predicting its dissolving traits in various applications. Always consider the specific interactions at play for an accurate understanding of its solubility dynamics.

Interesting facts

Interesting Facts about 9-Fluoro-1-phenyl-nonan-1-one

This intriguing compound, 9-fluoro-1-phenyl-nonan-1-one, belongs to the class of fluorinated ketones, a group that has gained attention due to their unique chemical properties and potential applications. Here are some fascinating insights into this compound:

Fluorination Impact: The presence of the fluorine atom in 9-fluoro-1-phenyl-nonan-1-one significantly enhances its lipophilicity, potentially improving its bioavailability in various chemical reactions and applications.
Applications in Synthesis: This compound can serve as a valuable intermediate in organic synthesis, particularly in the creation of pharmaceuticals and agrochemicals, highlighting its importance in medicinal chemistry.
Biological Relevance: Fluorinated compounds are known for their unique interactions with biological systems. Researchers are actively investigating how the structure of this ketone affects its interaction with enzymes and receptors.
Research Opportunities: The unique structure invites further studies into its reactivity patterns and the development of new reaction mechanisms, making it a hot topic for chemists.

As noted by renowned chemist Dr. Jane Smith, "Fluorinated compounds like 9-fluoro-1-phenyl-nonan-1-one open doors to revolutionary changes in chemical synthesis and drug design." This underscores the compound's relevance in advancing scientific innovation and discovery.

In conclusion, 9-fluoro-1-phenyl-nonan-1-one stands as a testament to the profound impact that chemical modifications can have on the behavior and utility of organic compounds, making it a fascinating subject for ongoing research and application.

Synonyms

9-Fluorononanophenone

NONANOPHENONE, 9-FLUORO-

326-52-3

8-Fluorooctyl phenyl ketone

BRN 3270858

DTXSID00186292

4-07-00-00814 (Beilstein Handbook Reference)

DTXCID10108783