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Atomfair 3-Phenyl-1,4,2-dioxazol-5-one C8H5NO3
Description 3-Phenyl-1,4,2-dioxazol-5-one (CAS No. 19226-36-9) is a high-purity heterocyclic organic compound with the molecular formula C8H5NO3. This specialized chemical features a dioxazolone core structure substituted with a phenyl group at the 3-position, making it a valuable intermediate for synthetic organic chemistry and pharmaceutical research. The compound is supplied as a crystalline solid with ??95% purity (HPLC) and is rigorously tested for consistency in quality and performance. Ideal for use in cycloaddition reactions, ring-opening transformations, and as a precursor for bioactive molecule synthesis. Packaged under inert gas to ensure stability and shipped with comprehensive analytical data (MSDS, NMR, HPLC).
Description
Description
3-Phenyl-1,4,2-dioxazol-5-one (CAS No. 19226-36-9) is a high-purity heterocyclic organic compound with the molecular formula C8H5NO3. This specialized chemical features a dioxazolone core structure substituted with a phenyl group at the 3-position, making it a valuable intermediate for synthetic organic chemistry and pharmaceutical research. The compound is supplied as a crystalline solid with ??95% purity (HPLC) and is rigorously tested for consistency in quality and performance. Ideal for use in cycloaddition reactions, ring-opening transformations, and as a precursor for bioactive molecule synthesis. Packaged under inert gas to ensure stability and shipped with comprehensive analytical data (MSDS, NMR, HPLC).
- CAS No: 19226-36-9
- Molecular Formula: C8H5NO3
- Molecular Weight: 163.13
- Exact Mass: 163.026943022
- Monoisotopic Mass: 163.026943022
- IUPAC Name: 3-phenyl-1,4,2-dioxazol-5-one
- SMILES: C1=CC=C(C=C1)C2=NOC(=O)O2
- Synonyms: 3-phenyl-1,4,2-dioxazol-5-one, 19226-36-9, 1,4,2-Dioxazol-5-one, 3-phenyl-, starbld0049466, SCHEMBL22426318
Application
3-Phenyl-1,4,2-dioxazol-5-one is primarily employed as a versatile building block in medicinal chemistry for the synthesis of nitrogen- and oxygen-containing heterocycles. It serves as a key precursor in the development of potential pharmacophores, particularly in antimicrobial and anti-inflammatory agent research. The compound’s reactivity in [3+2] cycloadditions makes it valuable for constructing complex molecular architectures. Researchers also utilize it in polymer chemistry as a crosslinking agent or monomer for functional materials.
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