3-(4-Nitrophenyl)-5-phenylisoxazole CAS 31108-56-2

Purity 97%+In StockPharmaceutical Standards
CAS No.31108-56-2
Molecular FormulaC15H10N2O3
Molecular Weight266.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(4-Nitrophenyl)-5-phenylisoxazole CAS 31108-56-2 chemical structure

Description

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.

CATO supplies 3-(4-Nitrophenyl)-5-phenylisoxazole (CAS 31108-56-2), a certified reference material (molecular formula C15H10N2O3, MW 266.25 g/mol) for analytical method development and quality control.

Based on its molecular formula C15H10N2O3, 3-(4-Nitrophenyl)-5-phenylisoxazole contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 266.25 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.

As a certified reference material (CRM), 3-(4-Nitrophenyl)-5-phenylisoxazole 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 FormulaC15H10N2O3
Molecular Weight266.25 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 DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1965
Nitrogen Atoms2

Related Nitrophenyl Standards

Recommended Standards

Why CATO?