1,5,7-Trimethyl-3-(4-nitrophenylethenyl)-8-phenyl-4,4-difluoroboradiazasindacene

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1,5,7-Trimethyl-3-(4-nitrophenylethenyl)-8-phenyl-4,4-difluoroboradiazasindacene

1,5,7-Trimethyl-3-(4-nitrophenylethenyl)-8-phenyl-4,4-difluoroboradiazasindacene | 1802553-26-9

Catalog Number F01-0124
Category BODIPY
Molecular Formula C26H22BF2N3O2
Molecular Weight 457.288
Catalog Number Size Price Quantity
F01-0124 -- $--

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
Storage Store at -20°C

1,5,7-Trimethyl-3-(4-nitrophenylethenyl)-8-phenyl-4,4-difluoroboradiazasindacene is a boron-containing organic compound with a complex molecular structure. This compound consists of a boron-difluoro group, a boradiazasindacene core, and various aromatic rings, including a nitrophenylethenyl group. Its unique structure provides high fluorescence properties, which make it highly useful in various chemical and biological applications. The presence of the nitrophenyl group enhances its electron acceptor ability, contributing to the compound's distinct optical and electronic characteristics. These properties are exploited in a range of scientific fields, including sensing, imaging, and catalysis.

One of the main applications of 1,5,7-Trimethyl-3-(4-nitrophenylethenyl)-8-phenyl-4,4-difluoroboradiazasindacene is in fluorescence sensing. Due to its ability to emit light upon excitation, this compound can serve as a sensitive probe for detecting various analytes, including ions, gases, and biomolecules. The compound’s fluorescence intensity changes upon interaction with specific substances, allowing for real-time detection in diverse environments. This makes it suitable for applications in environmental monitoring, diagnostics, and chemical analysis, where the accurate detection of low concentrations of target substances is critical.

Another important application is in biological imaging. The strong fluorescent emission of 1,5,7-Trimethyl-3-(4-nitrophenylethenyl)-8-phenyl-4,4-difluoroboradiazasindacene allows for its use in live cell imaging and tissue labeling. Its high photostability and solubility in biological environments make it a valuable tool for observing cellular processes, molecular interactions, and tissue-specific markers in biological research. The ability to track biological events over time with minimal signal degradation is a key advantage in molecular biology and medical diagnostics, including cancer research and neurology.

In addition to sensing and imaging, this compound is also useful in the field of catalysis. The boron atom in 1,5,7-Trimethyl-3-(4-nitrophenylethenyl)-8-phenyl-4,4-difluoroboradiazasindacene can facilitate various chemical reactions by acting as a catalyst. Its unique molecular structure enables it to participate in reactions such as carbon-carbon bond formation, oxidation, and reduction processes. These catalytic capabilities are valuable in organic synthesis, where efficient and selective reactions are essential for producing high-quality chemicals, pharmaceuticals, and materials.

Finally, 1,5,7-Trimethyl-3-(4-nitrophenylethenyl)-8-phenyl-4,4-difluoroboradiazasindacene is also being explored for its potential use in optoelectronic devices. The compound's excellent optical properties, such as fluorescence emission and electron transfer capabilities, make it a promising candidate for applications in light-emitting diodes (LEDs), solar cells, and organic light-emitting diodes (OLEDs). Its ability to absorb and emit light efficiently in these devices could contribute to the development of more efficient and versatile optoelectronic technologies.

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