CAS 82302-19-0
:4-amino-2-methylpyrimidine-5-carbothioamide
Description:
4-Amino-2-methylpyrimidine-5-carbothioamide is an organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. This compound features an amino group (-NH2) at the 4-position and a methyl group (-CH3) at the 2-position of the pyrimidine ring, contributing to its basicity and potential reactivity. The carbothioamide functional group (-C(S)NH2) at the 5-position introduces a thiocarbonyl moiety, which can participate in various chemical reactions, including nucleophilic attacks and condensation reactions. The presence of both amino and thiocarbonyl groups enhances its potential as a building block in medicinal chemistry and organic synthesis. This compound may exhibit biological activity, making it of interest in pharmaceutical research. Its solubility, stability, and reactivity can vary depending on the solvent and environmental conditions, which are important considerations for its practical applications.
Formula:C6H8N4S
InChI:InChI=1/C6H8N4S/c1-3-9-2-4(6(8)11)5(7)10-3/h2H,1H3,(H2,8,11)(H2,7,9,10)
SMILES:Cc1ncc(c(=N)[nH]1)C(=N)S
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Found 1 products.
4-Amino-2-methylpyrimidine-5-carbothioamide
CAS:<p>Versatile small molecule scaffold</p>Formula:C6H8N4SPurity:Min. 95%Molecular weight:168.22 g/mol
