CAS 22462-35-7
:5-Fluoro-6-methoxy-2(1H)-pyrimidinone
Description:
5-Fluoro-6-methoxy-2(1H)-pyrimidinone is a heterocyclic organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of a fluorine atom at the 5-position and a methoxy group (-OCH3) at the 6-position contributes to its unique chemical properties. This compound is typically a white to off-white solid and is soluble in polar organic solvents. It exhibits potential biological activity, making it of interest in pharmaceutical research, particularly in the development of antiviral and anticancer agents. The molecular structure allows for various interactions with biological targets, and its fluorine substitution can enhance metabolic stability. Additionally, the methoxy group can influence the compound's lipophilicity and overall pharmacokinetic profile. As with many pyrimidine derivatives, it may participate in hydrogen bonding and other interactions, which are crucial for its biological activity. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.
Formula:C5H5FN2O2
InChI:InChI=1S/C5H5FN2O2/c1-10-4-3(6)2-7-5(9)8-4/h2H,1H3,(H,7,8,9)
InChI key:InChIKey=ASGDDXBMJFMJMY-UHFFFAOYSA-N
SMILES:O(C)C1=C(F)C=NC(=O)N1
Synonyms:- 2(1H)-Pyrimidinone, 5-fluoro-4-methoxy-
- 2(1H)-Pyrimidinone,5-fluoro-4-methoxy- (8CI)
- 5-Fluoro-6-methoxy-2(1H)-pyrimidinone
- 2(1H)-Pyrimidinone, 5-fluoro-6-methoxy-
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