Methyl 5-(4-aminophenyl)isoxazole-3-carboxylate CAS 879216-18-9

Purity 97%+In StockPharmaceutical Standards
CAS No.879216-18-9
Molecular FormulaC11H10N2O3
Molecular Weight218.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 5-(4-aminophenyl)isoxazole-3-carboxylate CAS 879216-18-9 chemical structure

Description

Methyl 5-(4-aminophenyl)isoxazole-3-carboxylate (CAS 879216-18-9), molecular formula C11H10N2O3 and molecular weight 218.21 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C11H10N2O3, Methyl 5-(4-aminophenyl)isoxazole-3-carboxylate contains an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 218.21 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

As a certified reference material (CRM), Methyl 5-(4-aminophenyl)isoxazole-3-carboxylate meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC11H10N2O3
Molecular Weight218.21 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms2

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