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CAS 885521-80-2

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4-Bromo-1H-indazole-3-carboxylic acid

Description:
4-Bromo-1H-indazole-3-carboxylic acid is a chemical compound characterized by its indazole core, which is a bicyclic structure containing a five-membered ring fused to a six-membered ring. The presence of a bromine atom at the 4-position and a carboxylic acid functional group at the 3-position contributes to its unique reactivity and properties. This compound is typically a solid at room temperature and is soluble in polar solvents, which is common for carboxylic acids. It may exhibit acidic behavior due to the carboxylic acid group, allowing it to participate in various chemical reactions, such as esterification or amidation. Additionally, the bromine substituent can serve as a site for further functionalization, making it a valuable intermediate in organic synthesis. Its potential applications may include use in pharmaceuticals, agrochemicals, or as a building block in the development of novel materials. As with many brominated compounds, it is essential to handle it with care due to potential environmental and health impacts.
Formula:C8H5BrN2O2
InChI:InChI=1S/C8H5BrN2O2/c9-4-2-1-3-5-6(4)7(8(12)13)11-10-5/h1-3H,(H,10,11)(H,12,13)
InChI key:InChIKey=IQVZPISNPRYBGH-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1C=2C(NN1)=CC=CC2Br
Synonyms:
  • 1H-indazole-3-carboxylic acid, 4-bromo-
  • 4-Bromo-3-indazolecarboxylic acid
  • 4-Bromoindazole-3-carboxylic acid
  • 4-Bromo-1H-indazole-3-carboxylic acid
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