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Methyl 2-oxo-2H-pyran-3-carboxylate, 98%
Methyl 2-oxo-2H-pyran-3-carboxylate, 98%
Methyl 2-oxo-2H-pyran-3-carboxylate, 98%
Thermo Scientific Chemicals

Methyl 2-oxo-2H-pyran-3-carboxylate, 98%

CAS: 25991-27-9 | C7H6O4 | 154.121 g/mol
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Catalog number H25932.03
also known as H25932-03
Price (USD)
43.65
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Quantity:
1 g
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Price (USD)
43.65
Online Exclusive
47.90
Save 4.25 (9%)
Each
Chemical Identifiers
CAS25991-27-9
IUPAC Namemethyl 2-oxo-2H-pyran-3-carboxylate
Molecular FormulaC7H6O4
InChI KeyGJVZWOMUTYNUCE-UHFFFAOYSA-N
SMILESCOC(=O)C1=CC=COC1=O
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SpecificationsSpecification SheetSpecification Sheet
Assay (GC)≥97.5%
Identification (FTIR)Conforms
Melting Point (clear melt)70.0-76.0?C
Appearance (Color)Yellow to orange to brown
FormCrystals or powder or crystalline powder
Methyl 2-oxo-2H-pyran-3-carboxylate is used as a reagent to investigate alfa, beta-unsaturated carbonyl compounds for their cytotoxic profiles against oral human normal and tumor cells.

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
Methyl 2-oxo-2H-pyran-3-carboxylate is used as a reagent to investigate alfa, beta-unsaturated carbonyl compounds for their cytotoxic profiles against oral human normal and tumor cells.

Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Wang, H. C.; Jagtap, A. D.; Chang, P. T.; Liu, J. R.; Liu, C. P.; Tseng, H. W.; Chen, G. S.; Chern, J. W. Bioisosteric replacement of an acylureido moiety attached to an indolin-2-one scaffold with a malonamido or a 2/4-pyridinoylamido moiety produces a selectively potent Aurora-B inhibitor. Eur. J. Med. Chem. 2014, 84, 312-334.
  2. Slack, R. D.; Siegler, M. A.; Posner, G. H. Highly stereocontrolled and regiocontrolled syntheses of polyoxygenated [2.2. 2] oxabicyclic synthons. Tetrahedron Lett. 2013, 54 (46), 6267-6270.