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6-Fluoro-7-methylbenzo[a]anthracene

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Identification
Molecular formula
C19H13F
CAS number
.66793-26-2
IUPAC name
6-fluoro-7-methyl-benzo[a]anthracene
State
State

At room temperature, 6-fluoro-7-methylbenzo[a]anthracene is in a solid state.

Melting point (Celsius)
183.00
Melting point (Kelvin)
456.15
Boiling point (Celsius)
490.00
Boiling point (Kelvin)
763.15
General information
Molecular weight
264.31g/mol
Molar mass
264.3120g/mol
Density
1.0961g/cm3
Appearence

6-Fluoro-7-methylbenzo[a]anthracene appears as a crystalline solid with characteristic fluorescence under UV light. The compound generally has a yellowish hue.

Comment on solubility

Solubility of 6-fluoro-7-methyl-benzo[a]anthracene

The solubility of 6-fluoro-7-methyl-benzo[a]anthracene is a fascinating topic, particularly due to its intricate structure and the implications for its applications. This compound is known for its relatively low solubility in polar solvents, primarily due to its large polycyclic aromatic hydrocarbon (PAH) structure which hinders interactions with these solvents. Here are some key points to consider:

  • Solvent Compatibility: It exhibits higher solubility in non-polar solvents such as hexane and toluene.
  • Temperature Influence: As with many organic compounds, solubility can increase with temperature, allowing greater solvation at elevated temperatures.
  • Practical Applications: Its limited water solubility poses challenges for biological studies and environmental assessments, requiring careful consideration during experiments.

In summary, while 6-fluoro-7-methyl-benzo[a]anthracene is less soluble in polar solvents, it finds greater solubility in non-polar environments. This phenomenon emphasizes the importance of understanding solvent interactions when working with complex organic compounds.

Interesting facts

Interesting Facts About 6-Fluoro-7-Methyl-Benzo[a]anthracene

6-Fluoro-7-methyl-benzoaanthracene is a fascinating polycyclic aromatic hydrocarbon (PAH) that belongs to a class of compounds known for their intriguing chemical properties and biological activities. Here are some key points that make this compound particularly interesting:

  • Structure and Functionality: The incorporation of a fluorine atom and a methyl group into the anthracene structure enhances its chemical reactivity, making it a valuable model for studying electronic properties and interactions in organic materials.
  • Research Applications: This compound is often investigated for its potential photophysical properties, which can be harnessed in optoelectronics and organic semiconductors. Its ability to modulate light absorption and emission makes it a candidate for innovative technologies.
  • Cancer Research: PAHs, including this compound, are of significant interest in cancer research as they are often implicated in the mechanisms of mutagenesis and carcinogenesis. Studies focusing on their biological activities can contribute to understanding the impact of environmental pollutants.
  • Synthetic Challenges: The synthesis of 6-fluoro-7-methyl-benzoaanthracene may present challenges yet provides insight into synthetic methods in organic chemistry that can lead to other complex molecular architectures.

"The beauty of chemistry lies in the intricate dance of atoms and the stories they tell about our world." This sentiment resonates deeply with the study of compounds like 6-fluoro-7-methyl-benzoaanthracene. By delving into its properties and applications, chemists can unlock new pathways leading to advancements in material science and biology.

Overall, 6-fluoro-7-methyl-benzoaanthracene exemplifies the complexity and utility of chemical compounds, reinforcing the notion that every molecule holds the potential for new discoveries.

Synonyms
Benz(a)anthracene, 6-fluoro-7-methyl-
2541-68-6
6-Fluoro-7-methylbenz[a]anthracene
BRN 2532106
6-FLUORO-7-METHYLBENZ(A)ANTHRACENE
DTXSID80180071
DTXCID90102562
ytmjgwzzujcjpe-uhfffaoysa-n