Search
Element Search
Structure Search
Thermo Scientific Chemicals
5-Methylisoxazole-3-carboxylic acid, 98+%
CAS: 3405-77-4 | C5H5NO3 | 127.099 g/mol
Have Questions?
Change view
Catalog number L17577.14
also known as L17577-14
Price (TWD)Request A Quote
-
Quantity:
25 g
Chemical Identifiers
CAS3405-77-4
IUPAC Name5-methyl-1,2-oxazole-3-carboxylic acid
Molecular FormulaC5H5NO3
InChI KeyBNMPIJWVMVNSRD-UHFFFAOYSA-N
SMILESCC1=CC(=NO1)C(O)=O
View more
Specifications
Specification Sheet
Specification SheetProton NMRConforms
Water Content (Karl Fischer Titration)≤0.5%
Appearance (Color)White to off-white to pale yellow
FormPowder or crystals or crystalline powder
Assay from Supplier's CofA≥98.0% (GC)
It is a reactant for Click/aza-Michael or Click/oligomeric alkyl carbodiimide esterification reactions, preparation of aminopyrazole amide derivatives as Raf kinase inhibitors in melanoma cells and preparation of trifluoromethoxyphenyl(thiazolyl)pyrroles and other heterocycle-bearing polyfunctionalized pyrroles via chain heterocyclization.
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
It is a reactant for Click/aza-Michael or Click/oligomeric alkyl carbodiimide esterification reactions, preparation of aminopyrazole amide derivatives as Raf kinase inhibitors in melanoma cells and preparation of trifluoromethoxyphenyl(thiazolyl)pyrroles and other heterocycle-bearing polyfunctionalized pyrroles via chain heterocyclization.
Notes
Store at room temperature. Keep away from strong oxidizing agents.
It is a reactant for Click/aza-Michael or Click/oligomeric alkyl carbodiimide esterification reactions, preparation of aminopyrazole amide derivatives as Raf kinase inhibitors in melanoma cells and preparation of trifluoromethoxyphenyl(thiazolyl)pyrroles and other heterocycle-bearing polyfunctionalized pyrroles via chain heterocyclization.
Notes
Store at room temperature. Keep away from strong oxidizing agents.
RUO – Research Use Only
General References:
- B. Chandrakantha.; Prakash Shetty.; Vijesh Nambiyar.; Nishitha Isloor.; Arun M. Isloor. Synthesis, characterization and biological activity of some new 1,3,4-oxadiazole bearing 2-flouro-4-methoxy phenyl moiety.European Journal of Medicinal Chemistry. 2010, 45 (3),1206-1210 .
- Peter S. Dragovich.; Thomas J. Prins.; Ru Zhou.; Theodore O. Johnson.; Edward L. Brown.; Fausto C. Maldonado.; Shella A. Fuhrman.; Leora S. Zalman.; Amy K. Patick.; David A. Matthews.; Xinjun Hou.; James W. Meador III.; Rose Ann Ferr.; Stephen T. Worland. Structure-Based Design, Synthesis, and Biological Evaluation of Irreversible Human Rhinovirus 3C Protease Inhibitors. Part 7: Structure-Activity Studies of Bicyclic 2-Pyridone-Containing Peptidomimetics.Bioorg. Med. Chem. Lett. 2002, 12 (5),733-738 .