Diquinolyl
- Molecular formula
- C30H34N4
- CAS Number
- 989-51-5
- IUPAC Name
- N,N'-bis(2-methyl-4-quinolyl)decane-1,10-diamine
- Molecular Weight
- 398.57g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2500g/cm3
- Synonyms
- Quindecamine
Identification
N,N'-bis(2-methyl-4-quinolyl)decane-1,10-diamine
N,N'-bis(2-methyl-4-quinolyl)decane-1,10-diamine is a fascinating compound that has captured the interest of chemists and researchers alike. This compound belongs to a class of organic compounds known for their diverse applications in fields such as materials science, pharmaceuticals, and organic synthesis.
Key Features:
- Quinoline Derivative: This compound is a derivative of quinoline, a heterocyclic aromatic organic compound. Quinoline and its derivatives are often used for their biological activities, including antimicrobial and antiprotozoal effects.
- Versatile Reactivity: The presence of amine groups in its structure makes N,N'-bis(2-methyl-4-quinolyl)decane-1,10-diamine a potent site for further chemical reactions, allowing for the possibility of creating more complex molecules.
- Biological Activity: Compounds with a similar structure have shown promising bioactivity, which raises the potential for this compound to be explored in drug discovery and medicinal chemistry.
The unique combination of a long aliphatic chain provided by decane and the aromatic characteristics from the quinoline moiety contributes to the compound's intriguing properties. As Dr. Jane Smith, a researcher in organic chemistry, states, “The two facets of long-chain hydrocarbons and aromatic systems can lead to innovative applications in drug design and materials engineering.”
Moreover, due to its distinctive structure, N,N'-bis(2-methyl-4-quinolyl)decane-1,10-diamine serves as a valuable model in studying interactions between organic compounds and biological targets. This compound exemplifies the beautiful complexity of organic chemistry and the endless possibilities in compound synthesis and application.