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Structure of 129295-31-4
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6-Chloro-1H-indazole-3-carboxylic acid features a chlorine atom at the 6-position of the indazole scaffold, enhancing electron-withdrawing character and metabolic stability. The carboxylic acid group at the 3-position enables direct conjugation or derivatization in medicinal chemistry campaigns. This rigid heterocyclic core integrates readily into bioactive molecules requiring targeted polarity and hydrogen-bonding capacity.
6-Chloro-1H-indazole-3-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling direct incorporation into bioactive scaffolds via amide coupling or Suzuki-Miyaura cross-coupling. The chloro group facilitates further functionalization, while the carboxylic acid enables derivatization under standard conditions. Its bench-stable crystalline form supports reliable handling and purification in synthetic 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: