Description

1-Benzyl-1H-indazole-3-carboxylic acid (CAS No. 41354-03-4) is a high-purity organic compound with the molecular formula C₁₅H₁₂N₂O₂. This indazole derivative is characterized by a benzyl group attached to the nitrogen at the 1-position and a carboxylic acid functional group at the 3-position of the indazole ring. It is a valuable building block in medicinal chemistry and pharmaceutical research, particularly in the synthesis of heterocyclic compounds and bioactive molecules. The product is supplied as a white to off-white crystalline powder with ≥95% purity (HPLC), ensuring consistency for research applications. Proper storage at 2-8°C in a tightly sealed container is recommended to maintain stability.

Properties

• CAS Number: 41354-03-4
• Complexity: 328
• IUPAC Name: 1-benzylindazole-3-carboxylic acid
• InChI: InChI=1S/C15H12N2O2/c18-15(19)14-12-8-4-5-9-13(12)17(16-14)10-11-6-2-1-3-7-11/h1-9H,10H2,(H,18,19)
• InChI Key: CDRCOZFGMPTGBL-UHFFFAOYSA-N
• Exact Mass: 252.089877630
• Molecular Formula: C15H12N2O2
• Molecular Weight: 252.27
• SMILES: C1=CC=C(C=C1)CN2C3=CC=CC=C3C(=N2)C(=O)O
• Topological: 55.1
• Monoisotopic Mass: 252.089877630
• Synonyms: 1-Benzyl-1H-indazole-3-carboxylic acid, 41354-03-4, DTXSID80441811, DTXCID80392632, 1-benzylindazole-3-carboxylic Acid, 1-benzyl indazolyl-3-carboxylic acid, 1H-Indazole-3-carboxylic acid, 1-(phenylmethyl)-, MFCD01631170, 1-Benzyl-1H-indazole-3-carboxylicacid, Oprea1_818763, 1-benzyl-indazole-3-carboxylic, SCHEMBL1225871, CHEMBL3415691, ALBB-035387, AKOS000301960, 1-Benzyl-1H-indazole-3-carbonic acid, FB67563, DS-14597, DB-070180, AO-702/14733008

Application

1-Benzyl-1H-indazole-3-carboxylic acid serves as a key intermediate in the synthesis of pharmacologically active indazole derivatives. Researchers utilize this compound in the development of enzyme inhibitors and receptor modulators due to its heterocyclic scaffold. It is particularly relevant in medicinal chemistry for designing potential therapeutic agents targeting inflammatory and neurological pathways. The carboxylic acid moiety allows for further functionalization through amidation or esterification reactions.

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