CAS 32550-24-6

2(1H)-Pyrimidinone,6-amino-5-ethyl-

Description:

2(1H)-Pyrimidinone, 6-amino-5-ethyl- is a heterocyclic organic compound characterized by a pyrimidine ring structure, which is a six-membered ring containing two nitrogen atoms at the 1 and 3 positions. This compound features an amino group (-NH2) at the 6 position and an ethyl group (-C2H5) at the 5 position of the pyrimidinone ring. The presence of the amino group contributes to its basicity and potential reactivity, making it a candidate for various chemical reactions, including nucleophilic substitutions. The ethyl group enhances the lipophilicity of the molecule, which may influence its solubility and biological activity. This compound may exhibit properties relevant to pharmaceuticals, agrochemicals, or as a building block in organic synthesis. Its specific applications and reactivity can vary based on the functional groups present and the overall molecular structure. As with many pyrimidine derivatives, it may also participate in hydrogen bonding, affecting its interactions in biological systems.

Formula: C₆H₉N₃O

InChI: InChI=1S/C6H9N3O/c1-2-4-3-8-6(10)9-5(4)7/h3H,2H2,1H3,(H3,7,8,9,10)

InChI key: CZJGCEGNCSGRBI-UHFFFAOYSA-N

SMILES: CCC1=C(NC(=O)N=C1)N

Synonyms:

• 2(1H)-Pyrimidinone,4-amino-5-ethyl- (9CI)
• Cytosine, 5-ethyl- (8CI)
• 5-Ethylcytosine