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Structure of 885520-98-9
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6-Bromo-4-methyl-1H-indazole is a heterocyclic scaffold featuring a bromine substituent at the 6-position and a methyl group at the 4-position, enabling selective functionalization in medicinal chemistry. The electron-deficient indazole core supports transition metal-catalyzed coupling reactions, while its bench-stable nature facilitates handling under standard conditions. This compound serves as a key intermediate for bioactive molecule synthesis.
6-Bromo-4-methyl-1H-indazole serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions for C–C bond formation. The bromine substituent provides high reactivity in Suzuki, Stille, and Negishi couplings, while the methyl group enhances metabolic stability. Its bench-stable nature and compatibility with diverse functional groups facilitate efficient synthesis of complex heterocyclic scaffolds relevant to kinase inhibitors and other bioactive molecules.
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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: