Search
元素の検索
構造の検索
Thermo Scientific Chemicals
2-Phenyl-5-oxazolone, 97%
CAS: 1199-01-5 | C9H7NO2 | 161.16 g/mol
化学物質識別子
CAS1199-01-5
IUPAC Name2-phenyl-4,5-dihydro-1,3-oxazol-5-one
Molecular FormulaC9H7NO2
InChI KeyQKCKCXFWENOGER-UHFFFAOYSA-N
SMILESO=C1CN=C(O1)C1=CC=CC=C1
さらに表示
仕様
スペックシート
スペックシートAssay (GC)≥96.0%
Appearance (Color)Cream to yellow to orange to red to brown or pink
FormCrystals or powder or crystalline powder or fused solid or granules
Melting Point (clear melt)83.0-94.0?C
2-Phenyl-5-oxazolone is a reagent used as a masked glycine equivalent and for the formation of heterocyclic structures, it can be used to produce 4-benzylidene-2-phenyl-4H-oxazol-5-one.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2-Phenyl-5-oxazolone is a reagent used as a masked glycine equivalent and for the formation of heterocyclic structures, it can be used to produce 4-benzylidene-2-phenyl-4H-oxazol-5-one.
Solubility
Soluble in most common organic solvents.
Notes
Air Sensitive. Protect from heat. Store away from oxidizing agents.
2-Phenyl-5-oxazolone is a reagent used as a masked glycine equivalent and for the formation of heterocyclic structures, it can be used to produce 4-benzylidene-2-phenyl-4H-oxazol-5-one.
Solubility
Soluble in most common organic solvents.
Notes
Air Sensitive. Protect from heat. Store away from oxidizing agents.
RUO – Research Use Only
General References:
- Titus Kretzschmar.; Martin Geiser. Evaluation of antibodies fused to minor coat protein III and major coat protein VIII of bacteriophage M 13. Gene. 1995, 155, (1), 61-65.
- Christoph Rader.; Carlos F Barbas III. Phage display of combinatorial antibody libraries. Current Opinion in Biotechnology. 1997, 8, (4), 503-508.
- Protected glycine equivalent in heterocyclic synthesis: Synth. Commun., 18, 651 (1988):