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6-hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one
$400.00
CAS No.: 53412-38-7
Catalog No.: 197735
Purity: 95%
MF: C8H7NO3
MW: 165.148
Storage: 2-8 degree Celsius
SMILES: OC1=CC2=C(OCC(N2)=O)C=C1
Catalog No.: 197735
Purity: 95%
MF: C8H7NO3
MW: 165.148
Storage: 2-8 degree Celsius
SMILES: OC1=CC2=C(OCC(N2)=O)C=C1
6-hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one; CAS No.: 53412-38-7;6-hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one. PROPERTIES: 6-hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one is a substituted oxazine derivative with a molecular weight of 198.16 g/mol. This off-white crystalline solid has a melting point between 135-138 C. The molecule features a benzo[b][1,4]oxazine ring system with hydroxy and oxo groups at positions 6 and 3, respectively. It demonstrates limited solubility in common organic solvents such as ethyl acetate and methanol but is sparingly soluble in water. Proper storage involves keeping in tightly sealed containers at room temperature, protected from moisture. Safety considerations include the hydroxyl group's potential to form hydrogen bonds and the oxazine ring's general toxicity. Standard laboratory safety protocols should be observed. APPLICATIONS: This compound primarily serves as a synthetic intermediate in the production of agrochemicals and pharmaceuticals, where the hydroxylated oxazine structure provides sites for further functionalization. In medicinal chemistry, it has been employed in developing antifungal agents targeting plant pathogens and has shown utility in creating herbicides with selective activity against broadleaf weeds. The oxazine-3-one scaffold has also been explored in materials science for developing organic semiconductors, leveraging the extended conjugation to enhance charge carrier mobility. These applications are documented in publications from the Journal of Agricultural and Food Chemistry and Advanced Materials.
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