Quinoline yellow
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- Molecular formula
- C18H18Cl2N2
- CAS Number
- 8004-92-0
- IUPAC Name
- 7,10-diazoniatricyclo[8.4.0.02,7]tetradeca-1(14),2,4,6,10,12-hexaene;dichloride
- Molecular Weight
- 384.45g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3291g/cm3
- Synonyms
- DIQUAT DICHLORIDE
Identification
Interesting facts
Interesting Facts about 7,10-Diazoniatricyclo[8.4.0.02,7]tetradeca-1(14),2,4,6,10,12-hexaene; Dichloride
7,10-Diazoniatricyclo[8.4.0.02,7]tetradeca-1(14),2,4,6,10,12-hexaene; dichloride is a fascinating compound notable for its unique structural properties and potential applications. Here are some intriguing aspects:
- Structural Complexity: This compound features a bicyclic framework that comprises multiple interconnected rings. Such complexity plays a significant role in its reactivity and interaction with different chemical species.
- Applications in Materials Science: The unique electronic and structural properties open avenues in the development of advanced materials, particularly in areas of polymers and organic electronics.
- Potential Biological Activity: Compounds with similar structures are often studied for biological properties. There is potential for research into its effects on biological systems, paving the way for novel therapeutic agents.
- Synthesis Challenges: The synthesis of such compounds can be challenging due to the required precision in maintaining the ring structures. Learning about synthesis methods enhances understanding of organic reactions and mechanisms.
- Dichloride Significance: The dichloride form introduces two chlorine atoms into the molecule, which can drastically alter reactivity and solubility, impacting the compound’s applicability in various chemical reactions.
In summary, 7,10-diazoniatricyclo[8.4.0.02,7]tetradeca-1(14),2,4,6,10,12-hexaene; dichloride stands out for its structural intricacies and diverse potential applications. As a focus of ongoing research in both synthetic and applied chemistry, it embodies the complexity and challenge inherent in the study of modern chemical compounds.