CAS:1310918-28-5 | 3-Bromo-5-fluoro-4-nitrobenzonitrile

Introduction of CAS:1310918-28-5 | 3-Bromo-5-fluoro-4-nitrobenzonitrile

3-Bromo-5-fluoro-4-nitrobenzonitrile (3-BFN) is an aromatic nitrile compound with a wide range of applications, from organic synthesis to drug discovery. It is a versatile organic compound that can be used in a variety of reactions and processes. 3-BFN is a valuable precursor for a number of organic compounds, including dyes, pharmaceuticals, and other chemicals. It is also a useful reagent for the synthesis of a range of other compounds, such as heterocyclic compounds and organometallic complexes.

Specification of CAS:1310918-28-5 | 3-Bromo-5-fluoro-4-nitrobenzonitrile

Research Application of CAS:1310918-28-5 | 3-Bromo-5-fluoro-4-nitrobenzonitrile

Herbicide Resistance and Biotransformation

Research has explored the use of related compounds to 3-Bromo-5-fluoro-4-nitrobenzonitrile for enhancing herbicide resistance in plants and biotransformation processes. For instance, transgenic plants expressing a bacterial detoxification gene showed resistance to the herbicide bromoxynil, a compound with a similar structure, demonstrating the potential of genetic engineering for herbicide resistance (Stalker, Mcbride, & Malyj, 1988). Additionally, the anaerobic biodegradation of bromoxynil under various conditions highlights the environmental fate and microbial transformation of such compounds (Knight, Berman, & Häggblom, 2003).

Synthetic Applications and Radiolabeling

The compound and its derivatives have found use in synthetic chemistry and radiolabeling for medical imaging. A study on the preparation of the metabotropic glutamate receptor 5 (mGluR5) PET tracer [(18)F]FPEB, using a similar nitrobenzonitrile compound, underscores the utility of these chemicals in synthesizing radiotracers for neurological studies (Lim, Labaree, Li, & Huang, 2014). Moreover, the facile synthesis of 2-bromo-3-fluorobenzonitrile, a compound closely related to 3-Bromo-5-fluoro-4-nitrobenzonitrile, demonstrates its significance in chemical synthesis, offering insights into halodeboronation reactions of aryl boronic acids (Szumigala, Devine, Gauthier, & Volante, 2004).

Environmental Impact and Degradation

The environmental impact and degradation pathways of structurally similar compounds are crucial for understanding the fate of 3-Bromo-5-fluoro-4-nitrobenzonitrile in ecosystems. Studies have revealed the metabolism of the herbicide bromoxynil by soil bacteria, such as Klebsiella pneumoniae subsp. ozaenae, which can utilize bromoxynil as a nitrogen source, suggesting potential microbial routes for the degradation of related compounds (Mcbride, Kenny, & Stalker, 1986).

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