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Structure of 1167055-46-0
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4-Bromo-1H-indole-7-carbonitrile features a bromine substituent at the 4-position and a nitrile group at the 7-position of the indole core, enabling direct functionalization in cross-coupling and cyclization reactions. The electron-deficient indole scaffold enhances reactivity in palladium-catalyzed transformations. This bench-stable compound serves as a key intermediate for synthesizing biologically active heterocycles.
4-Bromo-1H-indole-7-carbonitrile serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its compatible bromo and nitrile functionalities. The molecule exhibits good bench stability and facilitates efficient functionalization at the indole core, supporting the synthesis of substituted heterocycles and advanced API 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: