CAS 111079-42-6
:6-Chloro-5-iodo-2-methyl-4(1H)-pyrimidinone
Description:
6-Chloro-5-iodo-2-methyl-4(1H)-pyrimidinone is a heterocyclic organic compound characterized by a pyrimidine ring, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of chlorine and iodine substituents at positions 6 and 5, respectively, contributes to its reactivity and potential applications in medicinal chemistry. The methyl group at position 2 enhances its lipophilicity, which can influence its biological activity and solubility. This compound may exhibit various pharmacological properties, making it of interest in drug development, particularly in the field of antiviral or anticancer agents. Its molecular structure allows for potential interactions with biological targets, and the halogen substituents can facilitate further chemical modifications. As with many pyrimidine derivatives, it may also participate in nucleophilic substitution reactions, making it a versatile intermediate in organic synthesis. Safety and handling precautions should be observed due to the presence of halogens, which can pose health risks.
Formula:C5H4ClIN2O
InChI:InChI=1S/C5H4ClIN2O/c1-2-8-4(6)3(7)5(10)9-2/h1H3,(H,8,9,10)
InChI key:InChIKey=SIDORYUWTWQBMA-UHFFFAOYSA-N
SMILES:IC1=C(Cl)NC(C)=NC1=O
Synonyms:- 6-Chloro-5-iodo-2-methyl-4(3H)-pyrimidinone
- 4(1H)-Pyrimidinone, 6-chloro-5-iodo-2-methyl-
- 6-Chloro-5-iodo-2-methyl-4(1H)-pyrimidinone
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