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Structure of 1408074-64-5
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Methyl 5-bromo-7-azaindole-6-carboxylate features a brominated azaindole core with a methyl ester at the C6 position, enabling direct incorporation into diverse heterocyclic scaffolds. The electron-deficient pyridine-like ring enhances reactivity in cross-coupling processes, while the bromide serves as a reliable handle for palladium-mediated transformations. This compound offers high stability under standard bench conditions and facilitates efficient access to functionalized indole derivatives in medicinal chemistry applications.
Methyl 5-bromo-7-azaindole-6-carboxylate serves as a versatile building block for the synthesis of bioactive heterocycles, enabling palladium-catalyzed cross-coupling reactions at the bromo position. The 7-azaindole core provides enhanced solubility and metabolic stability compared to indole analogs, while the ester functionality allows for selective derivatization. Its bench-stable nature and compatibility with standard synthetic protocols make it ideal for medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: