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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives Pyridinecarboxylic acids
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Pyridines and derivatives Pyridinecarboxylic acids and derivatives Pyridinecarboxylic acids

Methyl 6-Bromo-5-Hydroxy-2-Pyridinecarboxylate (CAS No. 170235-19-5): A Comprehensive Overview

The compound Methyl 6-bromo-5-hydroxy-2-pyridinecarboxylate (CAS No. 170235-19-5) is a significant organic compound with a diverse range of applications in various fields, including pharmaceuticals, agrochemicals, and material sciences. This compound belongs to the class of pyridine derivatives, which are widely studied due to their unique chemical properties and biological activities. The structure of Methyl 6-bromo-5-hydroxy-2-pyridinecarboxylate consists of a pyridine ring substituted with a bromine atom at position 6, a hydroxyl group at position 5, and a methyl ester group at position 2. These substituents play a crucial role in determining the compound's reactivity, stability, and potential for use in different industries.

Recent studies have highlighted the importance of Methyl 6-bromo-5-hydroxy-2-pyridinecarboxylate in the development of novel drugs targeting various diseases. For instance, researchers have explored its potential as an anti-inflammatory agent due to its ability to inhibit specific enzymes involved in inflammatory pathways. Additionally, the compound has shown promise in anticancer research, where it demonstrates selective cytotoxicity against cancer cells without significantly affecting normal cells. These findings underscore the compound's versatility and its potential to contribute to advancements in medicinal chemistry.

The synthesis of Methyl 6-bromo-5-hydroxy-2-pyridinecarboxylate involves a series of well-established organic reactions, including bromination, hydroxylation, and esterification. The choice of reaction conditions and reagents is critical to ensure high yields and purity of the final product. Recent advancements in catalytic methods have enabled more efficient and environmentally friendly syntheses of this compound, aligning with the growing demand for sustainable chemical processes.

In terms of physical properties, Methyl 6-bromo-5-hydroxy-2-pyridinecarboxylate exhibits a melting point of approximately 180°C and is sparingly soluble in water but readily soluble in organic solvents such as dichloromethane and ethyl acetate. These properties make it suitable for various chemical transformations and purification techniques commonly employed in organic synthesis.

The chemical stability of Methyl 6-bromo-5-hydroxy-2-pyridinecarboxylate has been extensively studied under different conditions. It is relatively stable under neutral conditions but can undergo hydrolysis in the presence of strong acids or bases. This behavior is crucial for understanding its behavior during storage and transportation as well as its application in industrial processes.

One of the most exciting developments involving Methyl 6-bromo-5-hydroxy-2-pyridinecarboxylate is its use as an intermediate in the synthesis of bioactive molecules. For example, it has been employed as a key building block in the construction of complex heterocyclic compounds with potential pharmacological activities. Its ability to undergo various nucleophilic substitutions and cross-coupling reactions makes it an invaluable tool for medicinal chemists.

Furthermore, recent research has explored the application of Methyl 6-bromo-5-hydroxy-2-pyridinecarboxylate in materials science, particularly in the development of advanced materials with tailored electronic properties. Its incorporation into polymer matrices has shown promise for creating materials with enhanced conductivity and stability, opening new avenues for its use in electronic devices.

In conclusion, Methyl 6-bromo-5-hydroxy-2-pyridinecarboxylate (CAS No. 170235-19-5) is a versatile compound with significant potential across multiple disciplines. Its unique chemical structure, combined with recent advancements in synthesis and application techniques, positions it as a key player in both academic research and industrial innovation. As ongoing studies continue to uncover new properties and uses for this compound, its importance in the chemical sciences is expected to grow further.

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• 54232-43-8(6-Bromo-5-methoxypyridine-2-carboxylic acid)
• 934-07-6(Methyl 5-bromo-1H-pyrrole-2-carboxylate)
• 350602-03-8(Methyl 4,6-dibromo-3-methoxypicolinate)
• 321601-48-3(methyl 6-bromo-3-hydroxypyridine-2-carboxylate)
• 945954-94-9(methyl 6-bromo-3-methoxypyridine-2-carboxylate)
• 170235-18-4(Methyl 6-bromo-5-methoxypicolinate)
• 321596-55-8(methyl 4,6-dibromo-3-hydroxypyridine-2-carboxylate)
• 64354-26-3(4,6-Dibromo-5-hydroxypicolinic acid)