2-Mercapto-3-methyl-3H-quinazolin-4-one, with the CAS number 1705-09-5, is a heterocyclic compound characterized by the presence of a quinazolinone core structure. This compound features a thiol (-SH) group, which contributes to its reactivity and potential applications in various chemical reactions, including nucleophilic substitutions and metal complexation. The methyl group at the 3-position enhances its lipophilicity, potentially influencing its biological activity and solubility. 2-Mercapto-3-methyl-3H-quinazolin-4-one exhibits properties typical of thiol-containing compounds, such as the ability to form disulfide bonds and participate in redox reactions. It may also exhibit biological activities, including antimicrobial or antioxidant properties, making it of interest in medicinal chemistry. The compound's stability and reactivity can be influenced by environmental factors such as pH and temperature. Overall, its unique structure and functional groups make it a valuable compound for research in organic synthesis and pharmacology.

2-MERCAPTO-3-METHYL-3H-QUINAZOLIN-4-ONE

1705-09-5: Timtec-Bb Sbb010030, Akos B020693, Buttpark 148\07-31, Art-Chem-Bb B020693, 2-mercapto-3-methylquinazolin-4(3H)-one, 3-methyl-2-sulfanylquinazolin-4(3H)-one

2-Mercapto-3-methyl-3H-quinazolin-4-one

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CAS 1705-09-5: 2-MERCAPTO-3-METHYL-3H-QUINAZOLIN-4-ONE

2-Mercapto-3-methyl-3H-quinazolin-4-one

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2-Mercapto-3-methylquinazolin-4(3H)-one

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2-MERCAPTO-3-METHYL-3H-QUINAZOLIN-4-ONE

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