![6,6-difluoro-8-oxo-6,8-dihydrobenzo[f]pyrido[1',2':3,4][1,3,5,2]triazaborinino[6,1-a]isoindol-5-ium-6-uide](https://resource.bocsci.com/structure/1519003-32-7.gif?v=2025011501)
6,6-difluoro-8-oxo-6,8-dihydrobenzo[f]pyrido[1',2':3,4][1,3,5,2]triazaborinino[6,1-a]isoindol-5-ium-6-uide | 1519003-32-7
Catalog Number | F01-0100 |
Category | BODIPY |
Molecular Formula | C17H10BF2N3O |
Molecular Weight | 321.094 |
Catalog Number | Size | Price | Quantity |
---|---|---|---|
F01-0100 | -- | $-- |
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Product Introduction
BODIPY dyes are used to generate fluorescent conjugates of proteins, nucleotides, oligonucleotides and dextrans, as well as to prepare fluorescent enzyme substrates, fatty acids, phospholipids, lipopolysaccharides, receptor ligands and polystyrene microspheres.
- Product Specification
- Application
Excitation | 649 |
Emission | 667 |
Storage | Store at -20°C |
6,6-difluoro-8-oxo-6,8-dihydrobenzo[f]pyrido[1',2':3,4][1,3,5,2]triazaborinino[6,1-a]isoindol-5-ium-6-uide is a complex heterocyclic compound that contains a boron atom integrated into a fused triazaborine system. This structure combines the stability and electronic properties of boron with the unique characteristics of aromatic heterocycles, making it useful in various fields of research, including materials science, drug development, and fluorescence technology. The compound is characterized by its distinctive difluoro and oxo functional groups, which contribute to its reactivity and fluorescence properties, making it an interesting candidate for scientific studies.
One of the key applications of 6,6-difluoro-8-oxo-6,8-dihydrobenzo[f]pyrido[1',2':3,4][1,3,5,2]triazaborinino[6,1-a]isoindol-5-ium-6-uide is in fluorescence imaging and sensing. The compound’s ability to fluoresce upon excitation makes it highly valuable for cellular imaging, allowing researchers to track biological processes in real-time. By incorporating this compound into fluorescent probes, it can be used for monitoring cellular events such as protein localization, cellular uptake, and intracellular signaling, which is critical for understanding complex biological mechanisms.
Another important application is in the development of boron-based materials for electronic and optoelectronic devices. The incorporation of boron into the triazaborine structure imparts desirable electronic properties, including stability and efficient charge transfer. This makes the compound an ideal candidate for use in organic light-emitting diodes (OLEDs), organic solar cells, and other optoelectronic materials. The fluorescence properties of the compound further enhance its applicability in devices that require precise light emission and detection, improving the performance and efficiency of these systems.
The compound is also promising in the field of drug discovery and molecular targeting. The unique triazaborine core, combined with its functional groups, may offer selective interactions with specific biomolecules, making it useful in the development of targeted therapies. Researchers can explore its potential as a ligand for drug-receptor binding studies, which could lead to the identification of new therapeutic agents for diseases where selective targeting is required, such as cancer or neurodegenerative conditions. Its fluorescence also provides an advantage in tracking drug distribution and bioavailability in vivo, facilitating the development of more effective treatments.
Finally, 6,6-difluoro-8-oxo-6,8-dihydrobenzo[f]pyrido[1',2':3,4][1,3,5,2]triazaborinino[6,1-a]isoindol-5-ium-6-uide holds promise in environmental sensing and monitoring. Due to its sensitivity to environmental changes, particularly pH and metal ion concentrations, the compound can be used as a fluorescent sensor for detecting pollutants or toxins in environmental samples. This application could be crucial for monitoring water quality, soil contamination, and air pollution, offering a non-invasive and highly sensitive method for environmental analysis.
Applications of Fluorescent Probes & Dyes
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