Pyranine
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- Molecular formula
- C20H11O10S3Na3
- CAS Number
- 6358-69-6
- IUPAC Name
- 7-[2-[bis[2-[(8-hydroxy-5-sulfo-quinoline-7-carbonyl)amino]ethyl]amino]ethylcarbamoyl]-8-hydroxy-quinoline-5-sulfonic acid
- Molecular Weight
- 524.44g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 2.0500g/cm3
- Synonyms
- O-TRENSOX
Identification
Interesting facts
Interesting Facts About 7-[2-[bis[2-[(8-hydroxy-5-sulfo-quinoline-7-carbonyl)amino]ethyl]amino]ethylcarbamoyl]-8-hydroxy-quinoline-5-sulfonic acid
This compound, a complex sulfonic acid derivative of quinoline, is notable for its multifaceted applications in various scientific fields. Here are some intriguing highlights:
- Biological Significance: The compound is derived from quinoline, a structure known for its biological activity. Quinoline derivatives have been investigated for their potential antibacterial, antifungal, and anticancer properties.
- Complex Structure: With multiple functional groups, including sulfonic and amino groups, this compound exhibits a high degree of complexity, making it an interesting study in organic synthesis and medicinal chemistry. Its intricate design allows for diverse interactions in biological settings.
- Imaging and Detection: Compounds bearing hydroxyl and sulfonic acid moieties are often utilized in the field of bioimaging. They serve as fluorescent markers, aiding in the visualization of various biological processes and cellular functions.
- Water-Soluble Phenotype: The presence of multiple sulfonate groups enhances water solubility, which is crucial for biological compatibility during application in drug formulations or as a biological probe.
- Research and Development: This compound is under investigation for its potential use in targeted drug delivery systems, where it may transport therapeutic agents more effectively to specific sites in the body, potentially revolutionizing treatment modalities.
Overall, the study of 7-[2-[bis[2-[(8-hydroxy-5-sulfo-quinoline-7-carbonyl)amino]ethyl]amino]ethylcarbamoyl]-8-hydroxy-quinoline-5-sulfonic acid not only enhances our understanding of quinoline chemistry but also opens new avenues for advancements in pharmacology and biochemical research.