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Structure of 143468-13-7
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6-Bromo-7-azaindole delivers a brominated heterocyclic scaffold with enhanced solubility and stability, ideal for cross-coupling reactions. The electron-deficient pyridine ring pairs effectively with palladium catalysts, while the bromine moiety serves as a reliable handle for further functionalization in medicinal chemistry and materials science applications.
6-Bromo-7-azaindole serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C6 position via palladium-catalyzed cross-coupling reactions. Its electron-deficient heterocyclic core enhances reactivity in Suzuki-Miyaura and Buchwald-Hartwig couplings, while maintaining bench stability and compatibility with common protecting groups. The molecule functions as a key scaffold for constructing bioactive indole derivatives and pharmaceutical intermediates.
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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: