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Atomfair 5-Amino-1H-indole-2-carboxylic acid C9H8N2O2

Description 5-Amino-1H-indole-2-carboxylic acid (CAS No. 152213-40-6) is a high-purity heterocyclic compound with the molecular formula C9H8N2O2. This indole derivative features an amino group at the 5-position and a carboxylic acid moiety at the 2-position, making it a versatile building block for organic synthesis and pharmaceutical research. The compound is supplied as a fine, off-white to light yellow crystalline powder with ??95% purity (HPLC). It is soluble in polar organic solvents such as DMSO and methanol but exhibits limited solubility in water. Store under inert conditions at 2-8??C to ensure long-term stability. Ideal for researchers developing novel indole-based compounds for medicinal…

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Description

Description

5-Amino-1H-indole-2-carboxylic acid (CAS No. 152213-40-6) is a high-purity heterocyclic compound with the molecular formula C9H8N2O2. This indole derivative features an amino group at the 5-position and a carboxylic acid moiety at the 2-position, making it a versatile building block for organic synthesis and pharmaceutical research. The compound is supplied as a fine, off-white to light yellow crystalline powder with ??95% purity (HPLC). It is soluble in polar organic solvents such as DMSO and methanol but exhibits limited solubility in water. Store under inert conditions at 2-8??C to ensure long-term stability. Ideal for researchers developing novel indole-based compounds for medicinal chemistry, agrochemicals, and material science applications.

  • CAS No: 152213-40-6
  • Molecular Formula: C9H8N2O2
  • Molecular Weight: 176.17
  • Exact Mass: 176.058577502
  • Monoisotopic Mass: 176.058577502
  • IUPAC Name: 5-amino-1H-indole-2-carboxylic acid
  • SMILES: C1=CC2=C(C=C1N)C=C(N2)C(=O)O
  • Synonyms: 5-amino-1H-indole-2-carboxylic acid, 152213-40-6, DTXSID80571743, DTXCID00522515, 825-971-5

Application

5-Amino-1H-indole-2-carboxylic acid serves as a key intermediate in the synthesis of biologically active indole derivatives, including kinase inhibitors and serotonin receptor modulators. Its bifunctional structure allows for selective modifications at both the amino and carboxyl groups, enabling the creation of diverse molecular scaffolds. Researchers utilize this compound in peptidomimetic studies and as a precursor for fluorescent probes targeting cellular imaging applications.

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