7-Fluoro-2-methyl-3H-quinazolin-4-one is a heterocyclic organic compound characterized by its quinazolinone structure, which features a fused benzene and pyrimidine ring system. The presence of a fluorine atom at the 7-position and a methyl group at the 2-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and is known for its potential biological activity, making it of interest in medicinal chemistry and drug development. It may exhibit various pharmacological effects, including antimicrobial or anticancer properties, although specific activities can vary based on structural modifications and the biological context. The compound's solubility, stability, and reactivity can be influenced by the functional groups present, particularly the fluorine atom, which can enhance lipophilicity and alter interaction with biological targets. As with many quinazolinone derivatives, it may also serve as a scaffold for further chemical modifications to optimize its therapeutic potential. Safety and handling precautions should be observed due to its chemical nature and potential biological effects.

7-FLUORO-2-METHYL-3H-QUINAZOLIN-4-ONE

194473-03-5: 7-Fluoro-2-methyl-3H-quinazolin-4-one is a heterocyclic organic compound characterized by its quinazolinone structure, which features a fused benzene and pyrimidine ring system. The presence of a fluorine atom at the 7-position and a methyl group at the 2-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and is known for its potential biological activity, making it of interest in medicinal chemistry and drug development. It may exhibit various pharmacological effects, including antimicrobial or anticancer properties, although specific activities can vary based on structural modifications and the biological context. The compound's solubility, stability, and reactivity can be influenced by the functional groups present, particularly the fluorine atom, which can enhance lipophilicity and alter interaction with biological targets. As with many quinazolinone derivatives, it may also serve as a scaffold for further chemical modifications to optimize its therapeutic potential. Safety and handling precautions should be observed due to its chemical nature and potential biological effects.

CAS 194473-03-5

7-FLUORO-2-METHYL-3H-QUINAZOLIN-4-ONE

7-Fluoro-2-methylquinazolin-4(3H)-one

Ref: IN-DA00ANJ3