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CAS 885521-49-3

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3-bromo-1H-indazole-5-carboxylic acid

Description:
3-Bromo-1H-indazole-5-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 3-position and a carboxylic acid functional group at the 5-position contributes to its reactivity and potential applications in medicinal chemistry. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the carboxylic acid group. Its molecular structure allows for various interactions, making it a candidate for studies in drug development, particularly in targeting specific biological pathways. The bromine substituent can also enhance the compound's biological activity or influence its pharmacokinetic properties. As with many indazole derivatives, it may exhibit interesting pharmacological properties, including anti-inflammatory or anticancer activities, although specific biological data would depend on empirical studies. Safety and handling precautions should be observed, as with all chemical substances, particularly those with halogen substituents.
Formula:C8H5BrN2O2
InChI:InChI=1S/C8H5BrN2O2/c9-7-5-3-4(8(12)13)1-2-6(5)10-11-7/h1-3H,(H,10,11)(H,12,13)
InChI key:InChIKey=RWQMEUDBXGKAER-UHFFFAOYSA-N
SMILES:BrC=1C=2C(=CC=C(C(O)=O)C2)NN1
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