CAS 1125-85-5
:3,4-dihydro-2H-1,3-benzoxazin-2-one
Description:
3,4-Dihydro-2H-1,3-benzoxazin-2-one, with the CAS number 1125-85-5, is a heterocyclic organic compound characterized by its benzoxazine structure, which features a fused benzene and oxazine ring. This compound typically appears as a white to pale yellow solid and is known for its potential applications in various fields, including materials science and medicinal chemistry. It exhibits moderate solubility in organic solvents and is relatively stable under standard conditions. The presence of the oxazine moiety contributes to its reactivity, particularly in polymerization processes, making it a valuable precursor in the synthesis of polybenzoxazines, which are known for their thermal stability and mechanical properties. Additionally, 3,4-dihydro-2H-1,3-benzoxazin-2-one may exhibit biological activity, although specific pharmacological properties would require further investigation. Overall, its unique structural features and reactivity make it a compound of interest in both research and industrial applications.
Formula:C8H7NO2
InChI:InChI=1/C8H7NO2/c10-8-9-5-6-3-1-2-4-7(6)11-8/h1-4H,5H2,(H,9,10)
SMILES:c1ccc2c(c1)CN=C(O)O2
Synonyms:- 2H-1,3-Benzoxazin-2-one, 3,4-dihydro-
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Found 4 products.
3,4-Dihydrobenzo[e][1,3]oxazin-2-one
CAS:<p>3,4-Dihydrobenzo[e][1,3]oxazin-2-one</p>Purity:95%Molecular weight:149.15g/mol3,4-Dihydro-benzo[e][1,3]oxazin-2-one
CAS:Formula:C8H7NO2Purity:95.0%Color and Shape:SolidMolecular weight:149.1493,4-Dihydrobenzo[e][1,3]oxazin-2-one
CAS:<p>3,4-Dihydrobenzo[e][1,3]oxazin-2-one is an organic compound that is used as a catalyst in the synthesis of pharmaceuticals. It reacts with halides and alkali metal to form quaternary ammonium salts. This reaction can be represented by the following scheme:</p>Formula:C8H7NO2Purity:Min. 95%Molecular weight:149.15 g/mol



