Skip to main content

1-(4-Fluorophenyl)hexane-1,5-dione

ADVERTISEMENT
Identification
Molecular formula
C12H13FO2
CAS number
368-21-6
IUPAC name
1-(4-fluorophenyl)hexane-1,5-dione
State
State

The compound is typically found in a solid state at room temperature. Its crystalline structure allows it to maintain a consistent form under standard conditions.

Melting point (Celsius)
44.00
Melting point (Kelvin)
317.15
Boiling point (Celsius)
295.00
Boiling point (Kelvin)
568.15
General information
Molecular weight
210.24g/mol
Molar mass
210.2360g/mol
Density
1.1041g/cm3
Appearence

1-(4-Fluorophenyl)hexane-1,5-dione appears as a crystalline solid. It may vary in color depending on the purity and specific conditions, often presenting as white to off-white. Crystalline solids such as this compound are generally opaque and possess a structured lattice arrangement.

Comment on solubility

Solubility of 1-(4-Fluorophenyl)hexane-1,5-dione

1-(4-Fluorophenyl)hexane-1,5-dione is a compound that demonstrates interesting solubility characteristics. Generally, the solubility of this compound can be influenced by the following factors:

  • Polarity: The presence of the fluorophenyl group can enhance the polarity of the molecule, which may positively affect its solubility in polar solvents.
  • Solvent Type: It tends to dissolve well in organic solvents such as ethanol and acetone, while exhibiting limited solubility in water due to its non-polar hydrocarbon chain.
  • Temperature: Like many organic compounds, the solubility of 1-(4-fluorophenyl)hexane-1,5-dione may increase with temperature; hence, raising the temperature can enhance its dissolution in suitable solvents.

In conclusion, it is essential to consider the solvent characteristics when determining the solubility of 1-(4-fluorophenyl)hexane-1,5-dione. Each solvent interacts differently with this compound, highlighting the importance of context in its solubility profile. As the great chemist Antoine Lavoisier once said, “Nothing is lost, nothing is created, everything is transformed,” and this applies aptly to the transformations of solubility depending on environmental conditions.

Interesting facts

Interesting Facts about 1-(4-Fluorophenyl)hexane-1,5-dione

1-(4-Fluorophenyl)hexane-1,5-dione is a fascinating compound that exhibits unique chemical properties and potential applications. Here are some intriguing insights into this compound:

  • Structural Insights: This molecule features a hexane backbone with a dione functional group, contributing to its reactivity and versatility in organic synthesis.
  • Utility in Organic Synthesis: The presence of the dione functional group makes this compound a useful intermediate in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals.
  • Fluorine's Effect: The 4-fluorophenyl group plays a significant role in enhancing the compound's biological activity and stability. Fluorine atoms can alter the electronic properties, making the compound more lipophilic and increasing its interaction with biological targets.
  • Biological Activities: Compounds with fluorinated aromatic systems are often studied for their medicinal properties; thus, this compound may possess interesting biological activities that warrant further investigation.
  • Research Opportunities: With ongoing research in the field of medicinal and organic chemistry, 1-(4-fluorophenyl)hexane-1,5-dione presents exciting opportunities for scientists to explore its potential applications and effects.

Overall, 1-(4-fluorophenyl)hexane-1,5-dione is a valuable compound with significant implications in the realms of chemistry and pharmacology. With its interesting structure and reactivity, it continues to be a subject of study for those interested in the synthesis and application of novel organic materials.

Synonyms
1,5-HEXANEDIONE, 1-(p-FLUOROPHENYL)-
BRN 2580560
1-(p-Fluorophenyl)-1,5-hexanedione
29229-59-2
DTXSID60183484
RefChem:221408
DTXCID70105975
1-p-Fluorphenylhexan-1,5-dion
SCHEMBL13564338