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CAS 89853-87-2

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4-amino-5-carboxy-2-ethyl-*mercaptopyrimidine cry

Description:
4-Amino-5-carboxy-2-ethylmercaptopyrimidine is a chemical compound characterized by its pyrimidine ring structure, which includes an amino group (-NH2), a carboxylic acid group (-COOH), and a mercapto group (-SH) attached to the pyrimidine core. This compound is typically a solid at room temperature and may exhibit properties such as solubility in polar solvents due to the presence of functional groups that can engage in hydrogen bonding. It is likely to have biological significance, potentially serving as an intermediate in the synthesis of pharmaceuticals or as a biochemical agent. The presence of the mercapto group suggests it may participate in redox reactions or form disulfide bonds, which can be relevant in biological systems. Additionally, the ethyl group contributes to its hydrophobic character, influencing its interaction with other molecules. Overall, this compound's unique combination of functional groups makes it a subject of interest in medicinal chemistry and biochemistry.
Formula:C7H9N3O2S
InChI:InChI=1/C7H9N3O2S/c1-2-13-7-9-3-4(6(11)12)5(8)10-7/h3H,2H2,1H3,(H,11,12)(H2,8,9,10)
SMILES:CCSc1ncc(c(=N)[nH]1)C(=O)O
Synonyms:
  • 4-Amino-5-carboxy-2-ethyl-mercaptopyrimidine
  • 4-Amino-2-(Ethylsulfanyl)Pyrimidine-5-Carboxylic Acid
  • 4-Amino-2-ethylthiopyrimidine-5-carboxylic acid
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