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CAS 56584-63-5

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4-aminopyrimidine-5-carbothioamide

Description:
4-Aminopyrimidine-5-carbothioamide is a heterocyclic organic compound characterized by its pyrimidine ring structure, which contains both an amino group and a carbothioamide functional group. The presence of the amino group at the 4-position and the carbothioamide at the 5-position contributes to its reactivity and potential biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amino group, which can engage in hydrogen bonding. Its chemical properties include the ability to participate in nucleophilic reactions, making it a candidate for various synthetic applications in medicinal chemistry. Additionally, derivatives of pyrimidine compounds are often investigated for their pharmacological properties, including antimicrobial and antitumor activities. The compound's CAS number, 56584-63-5, is a unique identifier that facilitates its identification in chemical databases and literature. Overall, 4-aminopyrimidine-5-carbothioamide is of interest in both synthetic and medicinal chemistry contexts.
Formula:C5H6N4S
InChI:InChI=1/C5H6N4S/c6-4-3(5(7)10)1-8-2-9-4/h1-2H,(H2,7,10)(H2,6,8,9)
SMILES:c1c(c(=N)[nH]cn1)C(=N)S
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