Search Thermo Fisher Scientific
Element Search
Structure SearchThermo Scientific Chemicals
5-Methylisoxazole-3-carboxylic acid, 98+%, Thermo Scientific Chemicals
Catalog number: L17577.14
25 g, Each
Thermo Scientific Chemicals
5-Methylisoxazole-3-carboxylic acid, 98+%, Thermo Scientific Chemicals
Catalog number: L17577.14
25 g, Each
Quantity
Catalog number: L17577.14
also known as L17577-14
Price (USD)
Price: 238.00
Online price: 203.65
Your price:
Quantity
-
Chemical Identifiers
CAS
3405-77-4
IUPAC Name
5-methyl-1,2-oxazole-3-carboxylic acid
Molecular Formula
C5H5NO3
InChI Key
BNMPIJWVMVNSRD-UHFFFAOYSA-N
SMILES
CC1=CC(=NO1)C(O)=O
Specifications
Specification SheetProton NMR
Conforms
Water Content (Karl Fischer Titration)
≤0.5%
Appearance (Color)
White to off-white to pale yellow
Form
Powder or crystals or crystalline powder
Assay from Supplier's CofA
≥98.0% (GC)
Description
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
Figures
Documents & Downloads
Certificates
Search by lot number or partial lot number
Frequently asked questions (FAQs)
Citations & References
Search citations by name, author, journal title or abstract text