| Chemical Name: | 4-Quinolinecarbonitrile, 2-bromo- |
| CAS Number: | 95104-24-8 |
| Product Number: | AG005TDG(AGN-PC-02TH85) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C10H5BrN2 |
| Molecular Weight: | 233.0641 |
2-Bromoquinoline-4-carbonitrile, also known as $name$, is a versatile compound widely used in chemical synthesis. In organic chemistry, it serves as a valuable building block for the preparation of various biologically active molecules and pharmaceutical intermediates. With its unique structural features, $name$ is particularly favored in the synthesis of heterocyclic compounds and complex organic frameworks.One of the key applications of 2-Bromoquinoline-4-carbonitrile lies in its role as a precursor for the synthesis of quinoline derivatives. By functionalizing the bromine and nitrile groups, chemists can access a diverse array of substituted quinoline derivatives with tailored properties and reactivities. These derivatives find applications in medicinal chemistry, agrochemicals, and material science, showcasing the versatility and importance of $name$ in organic synthesis.Additionally, 2-Bromoquinoline-4-carbonitrile can be utilized in transition metal-catalyzed cross-coupling reactions to construct carbon-carbon or carbon-heteroatom bonds. This methodology enables the efficient preparation of complex molecules with high regio- and stereo-selectivity, making $name$ a valuable tool for synthetic chemists working in drug discovery and materials science research.Overall, the strategic use of 2-Bromoquinoline-4-carbonitrile in chemical synthesis demonstrates its significance as a pivotal component in the construction of diverse molecular architectures with potential applications in various scientific fields.
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