Methyl 4-bromo-1H-indole-2-Carboxylate: A Versatile Intermediate
Exploring the properties, applications, and synthesis of a key building block in organic chemistry.
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Methyl 4-bromo-1H-indole-2-carboxylate
This compound serves as a critical building block in the synthesis of numerous complex organic molecules, particularly within the pharmaceutical industry. Its unique structure, featuring an indole core substituted with a bromine atom and a methyl carboxylate group, allows for diverse chemical transformations, making it invaluable for drug discovery and materials science.
- Explore the key properties of methyl 4-bromo-1H-indole-2-carboxylate, including its molecular formula C10H8BrNO2 and a molecular weight of 254.08.
- Understand the synthesis pathways for methyl 4-bromo-1H-indole-2-carboxylate to ensure efficient production.
- Discover the broad applications of methyl 4-bromo-1H-indole-2-carboxylate in advanced organic synthesis.
- Learn about the importance of cas 167479-13-2 as a specific identifier for this essential chemical intermediate.
Advantages Offered
Versatile Reactivity
Leverage the reactivity of methyl 4-bromo-1H-indole-2-carboxylate in various chemical synthesis reactions, crucial for creating novel compounds.
Pharmaceutical Intermediate
Utilize this compound as a vital component in the synthesis of pharmaceutical intermediates, advancing drug discovery efforts.
Building Block Utility
Employ this organic synthesis building block to construct intricate molecular architectures for cutting-edge materials and therapeutics.
Key Applications
Drug Discovery
Its role as a pharmaceutical intermediate makes it indispensable for researchers exploring new drug candidates and therapies.
Organic Synthesis
Serves as a versatile tool for chemists to create a wide array of organic molecules through various synthetic routes.
Materials Science
The compound's unique structure can be exploited in the development of novel materials with tailored properties.
Chemical Research
Essential for academic and industrial research laboratories investigating heterocyclic chemistry and reaction methodologies.