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11-fluoro-7-methylbenzo[c]acridine

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Identification
Molecular formula
C18H12FN
CAS number
133745-83-2
IUPAC name
11-fluoro-7-methyl-benzo[c]acridine
State
State

At room temperature, 11-fluoro-7-methylbenzo[c]acridine is a solid. It is not very volatile, which is typical for aromatic compounds of its nature.

Melting point (Celsius)
172.00
Melting point (Kelvin)
445.15
Boiling point (Celsius)
510.00
Boiling point (Kelvin)
783.15
General information
Molecular weight
279.32g/mol
Molar mass
279.3170g/mol
Density
1.2500g/cm3
Appearence

11-Fluoro-7-methylbenzo[c]acridine typically appears as a pale yellow crystalline solid. The compound has an aromatic structure that may give rise to its slight coloration.

Comment on solubility

Solubility of 11-fluoro-7-methyl-benzo[c]acridine

The solubility of 11-fluoro-7-methyl-benzo(c)acridine is a topic of interest due to its unique chemical structure and potential applications. Understanding the solubility of this compound can provide insights into its behavior in different solvents and environments.

Factors Influencing Solubility

Several factors influence the solubility of 11-fluoro-7-methyl-benzo(c)acridine:

  • Polarity: The presence of fluorine and the methyl group can significantly affect the overall polarity of the compound, impacting its solubility in polar vs. non-polar solvents.
  • Hydrogen Bonding: The ability to form hydrogen bonds with solvents can enhance solubility in particular environments.
  • Temperature: Typically, solubility increases with temperature; thus, evaluating solubility at varying temperatures is crucial for practical applications.

General Observations

While detailed solubility data for 11-fluoro-7-methyl-benzo(c)acridine may be limited, certain aspects can be considered:

  • It may exhibit better solubility in organic solvents compared to water due to its aromatic structure.
  • The fluorine substituent could enhance interactions with certain solvents, potentially increasing solubility.
  • Understanding its solubility profiles could aid in predicting its bioavailability and reactivity in chemical processes.

To sum up, while specific solubility data for 11-fluoro-7-methyl-benzo(c)acridine might require further experimental investigation, it is clear that factors such as polarity, hydrogen bonding, and temperature play pivotal roles in defining how this compound interacts with various solvents.

Interesting facts

Interesting Facts about 11-fluoro-7-methyl-benzo<c>acridine

11-fluoro-7-methyl-benzo<c>acridine is an intriguing chemical compound that belongs to the class of acridine derivatives. It exhibits various properties that make it a subject of interest in several fields of research, including medicinal chemistry and materials science. Here are some captivating insights into this fascinating compound:

  • Fluorine Impact: The presence of a fluorine atom significantly influences the chemical reactivity and biological activity of the compound. Fluorinated compounds often show enhanced lipophilicity, which can improve permeability in biological membranes, making them valuable in drug design.
  • Potential Biological Activity: Compounds like 11-fluoro-7-methyl-benzo<c>acridine have been studied for their potential as antitumor agents. Acridine derivatives are known for their ability to intercalate DNA, which can disrupt replication and transcription processes in cancer cells.
  • Utilization in Organic Synthesis: Due to its unique structure, this compound can serve as a building block for the synthesis of more complex molecules in organic chemistry. Its distinct functional groups can lead to diverse chemical transformations.
  • Environmental Considerations: As with many synthetic compounds, understanding the environmental impact of 11-fluoro-7-methyl-benzo<c>acridine is crucial. Researchers are investigating its degradation pathways and persistence in various ecosystems.
  • Applications in Materials Science: The optical and electronic properties of acridine derivatives have piqued the interest of materials scientists. Studies are being conducted to explore the use of compounds like this one in organic light-emitting diodes (OLEDs) and dye-sensitized solar cells.

The versatility of 11-fluoro-7-methyl-benzo<c>acridine emphasizes the importance of fluorinated compounds in modern chemistry, showcasing their potential to make impactful contributions across various scientific disciplines. Whether through enhancing drug efficacy or advancing material technologies, this compound represents the cutting-edge of chemical research.

Synonyms
439-25-8
BENZ(c)ACRIDINE, 11-FLUORO-7-METHYL-
11-fluoro-7-methylbenzo[c]acridine
7-Methyl-11-fluorobenz(c)acridine
1-Fluoro-10-methyl-7,8-benzacridine
DTXSID60195981