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Atomfair 6-Bromo-1H-indazole-3-carboxylic acid C8H5BrN2O2

Description 6-Bromo-1H-indazole-3-carboxylic acid (CAS No. 660823-36-9) is a high-purity heterocyclic organic compound with the molecular formula C8H5BrN2O2. This indazole derivative features a bromine substituent at the 6-position and a carboxylic acid functional group at the 3-position, making it a versatile building block for pharmaceutical and agrochemical research. With a molecular weight of 241.04 g/mol, this compound is ideal for Suzuki coupling reactions, amide bond formations, and other synthetic transformations. Suitable for researchers in medicinal chemistry, it is provided with comprehensive analytical data including HPLC, NMR, and MS to ensure quality and consistency. Store in a cool, dry place away from…

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Description

Description

6-Bromo-1H-indazole-3-carboxylic acid (CAS No. 660823-36-9) is a high-purity heterocyclic organic compound with the molecular formula C8H5BrN2O2. This indazole derivative features a bromine substituent at the 6-position and a carboxylic acid functional group at the 3-position, making it a versatile building block for pharmaceutical and agrochemical research. With a molecular weight of 241.04 g/mol, this compound is ideal for Suzuki coupling reactions, amide bond formations, and other synthetic transformations. Suitable for researchers in medicinal chemistry, it is provided with comprehensive analytical data including HPLC, NMR, and MS to ensure quality and consistency. Store in a cool, dry place away from light to maintain stability.

  • CAS No: 660823-36-9
  • Molecular Formula: C8H5BrN2O2
  • Molecular Weight: 241.04
  • Exact Mass: 239.95344
  • Monoisotopic Mass: 239.95344
  • IUPAC Name: 6-bromo-1H-indazole-3-carboxylic acid
  • SMILES: C1=CC2=C(C=C1Br)NN=C2C(=O)O
  • Synonyms: 6-bromo-1H-indazole-3-carboxylic acid, 660823-36-9, DTXSID90646113, DTXCID70596864, 816-169-6

Application

6-Bromo-1H-indazole-3-carboxylic acid is widely used as a key intermediate in the synthesis of biologically active compounds, particularly in drug discovery for oncology and inflammation targets. Its reactive carboxylic acid group allows for easy derivatization into amides, esters, and other functionalized indazole derivatives. Researchers utilize this compound in the development of kinase inhibitors and other small-molecule therapeutics due to its privileged indazole scaffold.

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