(5-Chloro-8-quinolinyl) acetate
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- Molecular formula
- C11H8ClNO2
- CAS Number
- 554-86-5
- IUPAC Name
- (5-chloro-8-quinolyl) acetate
- Molecular Weight
- 235.64g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4000g/cm3
- Synonyms
- chloroacetoxyquinoline
Identification
Interesting facts
Interesting Facts about (5-chloro-8-quinolyl) acetate
(5-chloro-8-quinolyl) acetate is a fascinating compound within the world of organic chemistry. Known for its unique structure, this compound has attracted attention for several reasons:
- Unique Structure: This compound features a quinoline backbone, characterized by a bicyclic aromatic structure that contributes to its chemical reactivity and stability. The incorporation of a chlorine atom at the 5-position adds an interesting twist, impacting both its electronic properties and its potential applications.
- Biological Activity: Compounds derived from quinoline structures are often explored in medicinal chemistry. They are known to exhibit a range of biological activities, including antibacterial, antiviral, and antimalarial properties. Research suggests that (5-chloro-8-quinolyl) acetate could potentially be investigated for similar therapeutic uses.
- Applications in Materials Science: The unique properties of (5-chloro-8-quinolyl) acetate make it an attractive candidate for various applications, such as in the development of dyes, pigments, and other specialty chemicals. Its ability to form complexes with metal ions is particularly notable.
- Research Potential: The ongoing studies into the reactivity and modifications of this compound could lead to the discovery of new derivatives with enhanced properties, expanding its applicability in pharmaceuticals and materials.
- Historical Significance: The quinoline family, from which this compound is derived, has a rich history in chemistry, with roots tracing back to the early 19th century. This lineage adds a historical dimension to its study, making it not just a modern compound but also a piece of chemical history.
In summary, (5-chloro-8-quinolyl) acetate stands as a compound of significant interest not just due to its chemical attributes but also due to its potential applications across various fields, making it a worthy subject for further exploration in the realm of chemistry.