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Acridin-2-ol

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Identification
Molecular formula
C13H9NO
CAS number
1193-71-9
IUPAC name
acridin-2-ol
State
State

At room temperature, acridin-2-ol exists as a solid.

Melting point (Celsius)
227.00
Melting point (Kelvin)
500.20
Boiling point (Celsius)
464.60
Boiling point (Kelvin)
737.80
General information
Molecular weight
195.22g/mol
Molar mass
195.2210g/mol
Density
1.2210g/cm3
Appearence

Acridin-2-ol typically appears as a pale yellow solid. This compound can also appear crystalline in pure form and is sensitive to light.

Comment on solubility

Solubility of Acridin-2-ol

Acridin-2-ol, with the chemical formula C13H9NO, exhibits interesting solubility characteristics that are essential for its various applications. Understanding the solubility of this compound can provide insight into its behavior in different environments:

  • Solvent Compatibility: Acridin-2-ol is generally soluble in polar solvents such as water and alcohols, which can enhance its utility in biological and chemical contexts.
  • Hydrophobic Properties: Despite its polar nature, acridin-2-ol contains a rigid aromatic structure that contributes to some hydrophobic character, making it less soluble in non-polar solvents.
  • pH Dependency: The solubility may be influenced by the pH of the surrounding solution, where increased acidity can lead to improved solubility due to protonation.

As a result, acridin-2-ol is often dissolved in solvents that balance both its polar and non-polar attributes, aiding in its use for synthesis, extraction, or biological applications. Understanding these solubility features is key to optimizing its usage in various scientific domains.

Interesting facts

Interesting Facts about Acridin-2-ol

Acridin-2-ol, a fascinating compound within the acridine family, serves as a prime example of the intersection of chemistry and applied sciences. This compound is primarily recognized for its role in various biological and pharmaceutical applications.

Key Insights:

  • Biological Significance: Acridin-2-ol has shown promise in medicinal chemistry and is often investigated for its potential as an antibacterial and antiviral agent. Researchers are keen on exploring its effects on various pathogens.
  • Fluorescent Properties: Due to its unique molecular structure, acridin-2-ol exhibits fluorescence, which makes it valuable in biochemical assays, particularly in tracing cellular events and mechanisms.
  • Environmental Impact: Its derivatives have been studied regarding their environmental persistence and potential toxicity, prompting discussions about ecological safety in various applications.
  • Synthetic Pathways: The synthesis of acridin-2-ol can involve multiple methods, from simple condensation reactions to more complex multi-step processes, showcasing the versatility of organic synthesis.

Quotes from Research:

As one research paper eloquently states, “The exploration of acridin derivatives reveals new horizons in drug development.” This sentiment highlights the compound's potential stretching beyond mere academic interest into practical applications.

Overall, acridin-2-ol exemplifies how chemical compounds can bridge various fields, from medicine to environmental science, illustrating the continual importance of studying organic molecules.

Synonyms
2-ACRIDINOL
3-Hydroxyacridine (European)
BRN 0142310
DTXSID90177371
5-21-04-00088 (Beilstein Handbook Reference)
RefChem:255123
DTXCID5099862
2-Hydroxyacridine
22817-17-0
acridine, 2-hydroxy-
SCHEMBL4435489
VUZCWTUAXNDZSX-UHFFFAOYSA-N