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Structure of 73907-98-9
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Methyl 6-amino-1H-indazole-7-carboxylate features a planar indazole core with strategically positioned amino and ester functionalities. The electron-rich aromatic system enables efficient coupling reactions, while the methyl ester group facilitates selective derivatization. This compound serves as a key intermediate in the synthesis of bioactive heterocycles and pharmaceutical candidates.
Methyl 6-amino-1H-indazole-7-carboxylate serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the 6-amino position and orthogonal manipulation of the ester group. Its bench-stable nature and compatibility with standard coupling reactions facilitate efficient synthesis of indazole-based scaffolds. The molecule functions as a key intermediate in constructing bioactive heterocycles, particularly for kinase inhibitors and targeted therapeutics.
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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: