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5,7-Dimethylbenzo[c]acridine

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Identification
Molecular formula
C19H15N
CAS number
188-61-2
IUPAC name
5,7-dimethylbenzo[c]acridine
State
State

At room temperature, 5,7-Dimethylbenzo[c]acridine is in the solid state, existing as a crystalline powder. It is stable under normal conditions and requires specific conditions to change to other states.

Melting point (Celsius)
178.00
Melting point (Kelvin)
451.15
Boiling point (Celsius)
554.00
Boiling point (Kelvin)
827.15
General information
Molecular weight
255.33g/mol
Molar mass
255.3290g/mol
Density
1.1869g/cm3
Appearence

5,7-Dimethylbenzo[c]acridine is an off-white to pale yellow crystalline solid. Its crystalline nature results in a defined structure which reflects light, giving it a shiny appearance. It is not soluble in water.

Comment on solubility

Solubility of 5,7-dimethylbenzo[c]acridine

5,7-dimethylbenzoacridine is a polycyclic aromatic hydrocarbon that exhibits unique solubility characteristics. Understanding its solubility behavior is crucial for applications in organic chemistry and material science. Here are some key points to consider:

  • Solvent Dependence: The solubility of 5,7-dimethylbenzoacridine can greatly vary depending on the solvent used. Typically, it shows enhanced solubility in non-polar solvents such as hexane or toluene.
  • Polar Solvents: In contrast, its solubility in polar solvents like water is minimal, as the compound is largely hydrophobic in nature.
  • Temperature Effect: Temperature can also impact solubility; generally, an increase in temperature leads to greater solubility for most organic compounds.
  • Applications: The solubility properties of 5,7-dimethylbenzoacridine are particularly relevant in fields such as pharmaceuticals and material synthesis, where its behavior in various solutions can influence performance.

In conclusion, while 5,7-dimethylbenzoacridine is relatively insoluble in water, it can dissolve effectively in non-polar solvents, making it a compound of interest in various applications. Understanding these solubility trends is essential for leveraging its properties in scientific research and industrial applications.

Interesting facts

Interesting Facts about 5,7-Dimethylbenzo[c]acridine

The compound 5,7-dimethylbenzo[c]acridine is a fascinating member of the acridine family, which is significant in various fields of chemical research. Here are some intriguing points about this compound:

  • Cyclic Structure: 5,7-dimethylbenzo[c]acridine features a unique fused ring system, which contributes to its distinct chemical properties. The fusion of benzene and acridine rings invites interesting studies in aromaticity and electronic structure.
  • Fluorescence: Many acridine derivatives are known for their luminescent properties. This compound shows promise in the field of photochemistry and materials science, particularly in the development of organic light-emitting devices (OLEDs).
  • Biological Activity: Compounds that share structural similarities with acridine have been studied for their potential as anti-cancer agents. Research has explored their ability to intercalate with DNA, which can affect cellular processes.
  • Synthetic Pathways: The synthesis of 5,7-dimethylbenzo[c]acridine can involve multi-step reactions, including reactions that form the foundational acridine structure. Chemists often tailor the synthesis route to achieve desired yields and purities.
  • Historical Significance: The acridine family, including this compound, has been a subject of study since the early 20th century, highlighting the ongoing interest in their chemical properties and potential applications.

As a chemist or student, delving into compounds like 5,7-dimethylbenzo[c]acridine opens a wealth of opportunities for research and application. It serves not only as a subject of theoretical study but also as a potential player in technological advancements such as drug development and materials science.

Synonyms
5,7-Dimethylbenz(c)acridine
CCRIS 7723
BENZ(c)ACRIDINE, 5,7-DIMETHYL-
5,7-dimethylbenz[c]acridine
BRN 0201562
DTXSID30147250
5-20-08-00538 (Beilstein Handbook Reference)
DTXCID6069741
10567-95-0