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CAS 179555-11-4

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6-Amino-4-methyl-3-pyridinecarboxylic acid

Description:
6-Amino-4-methyl-3-pyridinecarboxylic acid, also known as a derivative of pyridine, is characterized by its amino and carboxylic acid functional groups, which contribute to its potential as a biologically active compound. This substance typically appears as a crystalline solid and is soluble in water due to the presence of polar functional groups. The molecular structure includes a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom, and substituents that enhance its reactivity and interaction with biological systems. The amino group can participate in hydrogen bonding, making it relevant in various chemical reactions and biological applications. Additionally, the methyl group at the 4-position can influence the compound's lipophilicity and overall stability. This compound may be of interest in pharmaceutical research, particularly in the development of drugs targeting specific biological pathways. Its properties, such as melting point, boiling point, and specific reactivity, would need to be determined through experimental methods for precise applications.
Formula:C7H8N2O2
InChI:InChI=1S/C7H8N2O2/c1-4-2-6(8)9-3-5(4)7(10)11/h2-3H,1H3,(H2,8,9)(H,10,11)
InChI key:InChIKey=FBKFFOOSODQYPO-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1C(C)=CC(N)=NC1
Synonyms:
  • 2-Amino-5-carboxy-4-methylpyridine
  • 3-Pyridinecarboxylic acid, 6-amino-4-methyl-
  • 3-Pyridinecarboxylicacid,6-amino-4-methyl-(9CI)
  • 6-Amino-4-Methylpyridine-3-Carboxylic Acid
  • 6-Amino-4-methyl-3-pyridinecarboxylic acid
  • 6-Amino-4-methylnicotinic acid
  • 2-Amino-4-methyl-5-pyridinecarboxylic acid
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