Boron, [β-​(3,​5-​dimethyl-​2H-​pyrrol-​2-​ylidene-​κN)​-​3,​5-​dimethyl-​1H-​pyrrole-​2-​ethanolato-​κN1]​difluoro-​, (T-​4)-

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Boron, [β-​(3,​5-​dimethyl-​2H-​pyrrol-​2-​ylidene-​κN)​-​3,​5-​dimethyl-​1H-​pyrrole-​2-​ethanolato-​κN1]​difluoro-​, (T-​4)-

Boron, [β-​(3,​5-​dimethyl-​2H-​pyrrol-​2-​ylidene-​κN)​-​3,​5-​dimethyl-​1H-​pyrrole-​2-​ethanolato-​κN1]​difluoro-​, (T-​4)- | 1256494-55-9

Catalog Number F01-0092
Category BODIPY
Molecular Formula C14H17BF2N2O
Molecular Weight 278.11
Catalog Number Size Price Quantity

Product Introduction

A fluorescent probe for HClO.

  • Product Specification
  • Application
Excitation 649
Emission 667
Storage Store at -20°C

Boron [β-​(3,​5-​dimethyl-​2H-​pyrrol-​2-​ylidene-​κN)​-​3​,5-​dimethyl-​1H-​pyrrole-​2-​ethanolato-​κN1]​difluoro-​ (T-​4)- is a boron-containing compound with several distinctive applications in scientific research and industry.

Organic Light-Emitting Diodes (OLEDs): This boron compound is employed as a luminescent material in the development of OLEDs. Its unique electronic properties contribute to high efficiency and brightness in display technologies. By integrating such compounds into OLED structures, manufacturers can create more energy-efficient screens with improved color quality.

Chemical Sensors: The compound's sensitivity to environmental changes makes it suitable for use in chemical sensors. These sensors can detect volatile organic compounds or changes in humidity, which is valuable for various industrial and environmental monitoring applications. By leveraging its responsive nature, researchers can develop sophisticated sensing devices for precise data collection.

Catalysis: In coordination chemistry, this boron compound can serve as a catalyst in organic synthesis. It has the potential to facilitate a variety of chemical reactions, including polymerization and coupling reactions. Utilizing such catalysts helps in achieving higher yields and selectivity, thus optimizing the efficiency of chemical processes.

Photodynamic Therapy (PDT): The compound's photophysical properties make it a candidate for use in photodynamic therapy, particularly in targeting cancer cells. When activated by light, it generates reactive oxygen species, which can damage cellular components and ultimately lead to cell death. This targeted approach minimizes damage to healthy tissues and provides a promising avenue for localized cancer treatment.

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