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Structure of 1031417-71-6
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5-Bromo-3,7-dimethyl-1H-indazole delivers a sterically hindered, electron-deficient heterocyclic scaffold ideal for transition-metal-catalyzed coupling reactions. The bromine at the 5-position enables direct functionalization, while the methyl groups at C3 and C7 enhance solubility and stability under standard conditions. This compound serves as a key building block in medicinal chemistry and materials science.
5-Bromo-3,7-dimethyl-1H-indazole serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the bromine site via palladium-catalyzed cross-coupling reactions. The methyl groups at C3 and C7 enhance metabolic stability and modulate electronic properties, while the indazole core provides a rigid, hydrogen-bonding scaffold suitable for target engagement. Bench-stable and readily purified by chromatography, it facilitates efficient access to diverse heterocyclic architectures in API 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: