2,6-Diaminoacridine
- Molecular formula
- C13H11N3
- CAS Number
- 492-54-4
- IUPAC Name
- acridine-2,6-diamine
- Molecular Weight
- 211.26g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2238g/cm3
- Synonyms
- Acridine-2, 6-diamine
Identification
Interesting Facts About Acridine-2,6-diamine
Acridine-2,6-diamine, a fascinating nitrogen heterocyclic compound, is primarily recognized for its valuable contributions to various fields, including biology, chemistry, and materials science.
Key Characteristics and Applications
- Pharmaceutical Relevance: Acridine derivatives, including acridine-2,6-diamine, are significant in medicinal chemistry. They exhibit antimicrobial and anti-cancer properties, making them a subject of study for developing new therapeutic agents.
- Dye Production: This compound is also utilized in creating dyes and pigments due to its vibrant chromophore structure, which can absorb and emit light at specific wavelengths.
- Research Tool: Acridine-2,6-diamine serves as an important research tool in molecular biology and biochemistry, particularly in fluorescence studies and as a probe for nucleic acids.
Unique Features
What sets acridine-2,6-diamine apart are its structural properties. The presence of amino groups at the 2 and 6 positions enhances its reactivity and makes it suitable for various chemical reactions, leading to:
- Increased solubility in polar solvents
- Ability to form strong hydrogen bonds, crucial for interactions with biological macromolecules
Quote to Reflect
As a scientist once said, "The beauty of acridine derivatives lies in their versatility; they bridge the gap between chemistry and biology." These small yet powerful compounds open new doors in research and application.
In summary, acridine-2,6-diamine stands as a testament to the interplay between structure and function, continuing to pique the interest of researchers across various disciplines.