2-Phenyl-5-oxazolone, 97%, Thermo Scientific Chemicals
2-Phenyl-5-oxazolone, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

2-Phenyl-5-oxazolone, 97%, Thermo Scientific Chemicals

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Quantity:
1 g
5 g
25 g
Catalog number L00194.03
also known as L00194-03
Price (USD)/ Each
69.80
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Quantity:
1 g
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Price (USD)/ Each
69.80
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2-Phenyl-5-oxazolone, 97%, Thermo Scientific Chemicals
Catalog numberL00194.03
Price (USD)/ Each
69.80
-
Add to cart
Chemical Identifiers
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
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Cream to yellow to orange to red to brown or pink
FormCrystals or powder or crystalline powder or fused solid or granules
Assay (GC)≥96.0%
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.
RUO – Research Use Only

General References:

  1. 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.
  2. Christoph Rader.; Carlos F Barbas III. Phage display of combinatorial antibody libraries. Current Opinion in Biotechnology. 1997, 8, (4), 503-508.
  3. Protected glycine equivalent in heterocyclic synthesis: Synth. Commun., 18, 651 (1988):