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CAS 67130-67-0

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

Description:
6-Amino-5-(chloroacetyl)-1-ethylpyrimidine-2,4(1H,3H)-dione is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic heterocycle containing nitrogen atoms. This compound features an amino group at the 6-position and a chloroacetyl substituent at the 5-position, contributing to its reactivity and potential biological activity. The presence of the ethyl group at the 1-position enhances its lipophilicity, which may influence its pharmacokinetic properties. The dione functionality indicates the presence of two carbonyl groups, which can participate in various chemical reactions, including nucleophilic attacks and condensation reactions. This compound is of interest in medicinal chemistry, particularly for its potential applications in drug development, as modifications to the pyrimidine scaffold can lead to compounds with diverse biological activities. Its CAS number, 67130-67-0, allows for easy identification in chemical databases and literature. Overall, this compound exemplifies the structural diversity and functional potential found within pyrimidine derivatives.
Formula:C8H10ClN3O3
InChI:InChI=1/C8H10ClN3O3/c1-2-12-6(10)5(4(13)3-9)7(14)11-8(12)15/h2-3,10H2,1H3,(H,11,14,15)
SMILES:CCn1c(c(C(=O)CCl)c(nc1=O)O)N
Synonyms:
  • 2,4(1H,3H)-Pyrimidinedione, 6-amino-5-(2-chloroacetyl)-1-ethyl-
  • 67130-67-0
  • 6-Amino-5-(chloroacetyl)-1-ethylhydantoin
  • T6Nvmvj A2 Ev1G Fz [Wln]
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