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Structure of 1363380-96-4
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This brominated indazole carboxylic acid integrates a methyl group at the nitrogen and a bromine substituent at the five-position, enhancing electronic and steric profile for use in bioactive molecule synthesis. The carboxylic acid functionality enables direct coupling reactions, while the scaffold offers metabolic stability and favorable solubility under standard conditions.
5-Bromo-1-methyl-1H-indazole-3-carboxylic acid serves as a versatile building block for medicinal chemistry and heterocyclic synthesis, enabling direct functionalization at the C3 carboxylic acid and C5 bromine sites. Its bench-stable nature facilitates coupling reactions, including Suzuki-Miyaura and Buchwald-Hartwig transformations, while the methyl group enhances solubility and modulates electronic properties. The molecule functions as a key scaffold in the development of kinase inhibitors and other bioactive compounds.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: