
5,10,15-tris(4-bromophenyl)corrole | 326472-04-2
Catalog Number | A14-0054 |
Category | Calcium, Chloride and Other indicators |
Molecular Formula | C37H23Br3N4 |
Molecular Weight | 763.329 |
Catalog Number | Size | Price | Quantity |
---|---|---|---|
A14-0054 | -- | $-- |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
5,10,15-tris(4-bromophenyl)corrole is an incredibly potent and remarkably versatile compound that emerges as a paramount entity extensively employed in the realm of biomedicine. Its unparalleled configuration and chemical attributes render it a highly auspicious contender for combating a myriad of ailments, encompassing cancer and disorders of the neurological nature. This particular product manifests extraordinary efficacy in the curtailment of tumor proliferation, while simultaneously possessing neuroprotective qualities.
- Product Specification
- Application
Storage | Store at -20°C |
5,10,15-tris(4-bromophenyl)corrole is a specialized chemical compound with potential uses in various scientific fields. Here are some key applications of 5,10,15-tris(4-bromophenyl)corrole:
Photodynamic Therapy: This compound shows promise in photodynamic therapy (PDT) for cancer treatment. When activated by light, it can generate reactive oxygen species that destroy cancer cells, minimizing damage to surrounding healthy tissues. Researchers are exploring its use in treating tumors that are accessible to light exposure.
Catalysis: 5,10,15-tris(4-bromophenyl)corrole can serve as a catalyst in chemical reactions, particularly in oxidation processes. Its unique structural properties allow it to facilitate selective transformations, offering potential for green chemistry applications. By optimizing reaction conditions, this compound can enhance efficiency and selectivity in industrial processes.
Material Science: In material science, this corrole derivative can be incorporated into organic semiconductors and sensors. Its electronic properties make it valuable for developing components in optoelectronic devices, such as organic light-emitting diodes (OLEDs) and photodetectors. This opens avenues for advancements in flexible and wearable technology.
Porphyrin Chemistry: As a member of the corrole family, this compound is studied within the broader context of porphyrin chemistry for its ability to coordinate with metals. It can form stable complexes with metals, offering potential applications in areas like environmental sensing and catalysis. Researchers utilize its coordination properties to develop innovative metal-organic frameworks and other complex materials.
Recommended Services
Blogs & Technical Articles

- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- BODIPY Dyes: Definition, Structure, Synthesis and Uses
- Cyanine Dyes: Definition, Structure, Types and Uses
- Fluorescein Dyes: Definition, Structure, Synthesis and Uses
- Rhodamine Dyes: Definition, Structure, Uses, Excitation and Emission
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
- DNA Staining: Definition, Procedures, Benefits, Dyes and Uses
- Cell Staining: Definition, Principles, Protocols, Dyes, and Uses
- Ion Imaging: Definition, Principles, Benefits, Dyes, and Uses
- Fluorescent Labeling: Definition, Principles, Types and Applications
Recommended Products