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CAS 100130-05-0

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5-amino-2-(methylsulfanyl)pyrimidine-4-carboxylic acid

Description:
5-Amino-2-(methylsulfanyl)pyrimidine-4-carboxylic acid is an organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms. This compound features an amino group (-NH2) and a carboxylic acid group (-COOH), contributing to its polar nature and potential for hydrogen bonding. The presence of a methylthio group (-S-CH3) enhances its reactivity and solubility in polar solvents. This compound is often studied for its biological activity, particularly in the context of pharmaceuticals and agrochemicals, due to its structural similarity to nucleobases and its potential role in metabolic pathways. Its molecular structure allows for various interactions with biological macromolecules, making it of interest in medicinal chemistry. Additionally, the compound's stability and reactivity can be influenced by environmental factors such as pH and temperature, which are important considerations in its application and storage. Overall, 5-amino-2-(methylsulfanyl)pyrimidine-4-carboxylic acid is a versatile compound with significant implications in chemical and biological research.
Formula:C6H7N3O2S
InChI:InChI=1/C6H7N3O2S/c1-12-6-8-2-3(7)4(9-6)5(10)11/h2H,7H2,1H3,(H,10,11)
SMILES:CSc1ncc(c(C(=O)O)n1)N
Synonyms:
  • 4-Pyrimidinecarboxylic Acid, 5-Amino-2-(Methylthio)-
  • 5-Amino-2-(methylthio)pyrimidine-4-carboxylicacid
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