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Structure of 885278-24-0
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6-Bromo-1H-indazole-3-carbonitrile features a bromine substituent at the 6-position and a nitrile group at the 3-position of the indazole core. This combination imparts enhanced reactivity for cross-coupling transformations and facilitates downstream functionalization in medicinal chemistry and materials synthesis. The molecule exhibits good stability under standard handling conditions.
6-Bromo-1H-indazole-3-carbonitrile serves as a versatile building block for heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal functionalization profile. The bromo and nitrile groups facilitate sequential transformations, supporting the construction of complex indazole-based scaffolds with high regiocontrol. Its bench-stable nature and compatibility with standard reaction conditions make it suitable for medicinal chemistry and process development workflows.
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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: