
CAS 93456-61-2
:2(1H)-Pyrimidinone, 6-amino-5-(4-chlorophenyl)-4-ethyl-
Description:
2(1H)-Pyrimidinone, 6-amino-5-(4-chlorophenyl)-4-ethyl- is a chemical compound characterized by its pyrimidinone core structure, which features a six-membered aromatic ring containing nitrogen atoms. The presence of an amino group at the 6-position and a 4-chlorophenyl substituent at the 5-position contributes to its biological activity and potential pharmacological properties. The ethyl group at the 4-position enhances its lipophilicity, which can influence its solubility and permeability in biological systems. This compound may exhibit various properties such as being a potential intermediate in organic synthesis or having applications in medicinal chemistry, particularly in the development of pharmaceuticals. Its specific interactions and reactivity can be influenced by the electronic effects of the substituents, making it a subject of interest for further research in drug design and development. As with many pyrimidine derivatives, it may also show activity against certain biological targets, warranting investigation into its therapeutic potential.
Formula:C12H12ClN3O
Synonyms:- 6-Amino-5-(4-chlorophenyl)-4-ethylpyrimidin-2(1H)-one trifluoroacetate salt
- 4-Amino-5-(4-chlorophenyl)-6-ethyl-1,2-dihydropyrimidin-2-one
- 6-amino-5-(4-chlorophenyl)-4-ethylpyrimidin-2-(1H)-one
- 2(1H)-Pyrimidinone, 6-amino-5-(4-chlorophenyl)-4-ethyl-
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