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Structure of 1217090-32-8
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N-Methyl-5-bromo-4,7-diazaindole is a bench-stable heterocyclic scaffold featuring a bromine substituent at the 5-position and a methyl group on the nitrogen. This electron-deficient core integrates readily into cross-coupling reactions, enabling efficient access to functionalized indole derivatives for medicinal chemistry and materials applications.
N-Methyl-5-bromo-4,7-diazaindole serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the bromo position via palladium-catalyzed cross-coupling reactions. The molecule's diazaindole core provides enhanced solubility and metabolic stability compared to indole analogs, while the N-methyl group improves lipophilicity and cellular permeability. Bench-stable and readily purified by column chromatography, it functions effectively in the construction of complex heterocyclic scaffolds relevant to kinase inhibitors and CNS-targeted therapeutics.
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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: