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CAS 22365-19-1

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6-amino-5-(chloroacetyl)-1-methylpyrimidine-2,4(1H,3H)-dione

Description:
6-Amino-5-(chloroacetyl)-1-methylpyrimidine-2,4(1H,3H)-dione, with the CAS number 22365-19-1, is a pyrimidine derivative characterized by the presence of an amino group and a chloroacetyl substituent. This compound features a methyl group at the 1-position and two carbonyl groups at the 2 and 4 positions of the pyrimidine ring, contributing to its diketone nature. The chloroacetyl group enhances its reactivity, making it a potential candidate for various chemical reactions, including acylation and nucleophilic substitution. The amino group can participate in hydrogen bonding and may influence the compound's solubility and biological activity. Typically, compounds of this class are studied for their pharmacological properties, including antimicrobial and antitumor activities. The structural features of this compound suggest it may interact with biological targets, making it of interest in medicinal chemistry. Its stability, solubility, and reactivity can vary based on environmental conditions, such as pH and solvent polarity.
Formula:C7H8ClN3O3
InChI:InChI=1/C7H8ClN3O3/c1-11-5(9)4(3(12)2-8)6(13)10-7(11)14/h2,9H2,1H3,(H,10,13,14)
SMILES:Cn1c(c(C(=O)CCl)c(nc1=O)O)N
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