5-(Phenoxymethyl)-3-phenyl-1,2-oxazole CAS 35121-46-1

Purity 97%+In StockPharmaceutical Standards
CAS No.35121-46-1
Molecular FormulaC16H13NO2
Molecular Weight251.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(Phenoxymethyl)-3-phenyl-1,2-oxazole CAS 35121-46-1 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 5-(Phenoxymethyl)-3-phenyl-1,2-oxazole.

CATO supplies 5-(Phenoxymethyl)-3-phenyl-1,2-oxazole (CAS 35121-46-1), a certified reference material (molecular formula C16H13NO2, MW 251.28 g/mol) for analytical method development and quality control.

Based on its molecular formula C16H13NO2, 5-(Phenoxymethyl)-3-phenyl-1,2-oxazole 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 251.28 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), 5-(Phenoxymethyl)-3-phenyl-1,2-oxazole 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 FormulaC16H13NO2
Molecular Weight251.28 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1967
Nitrogen Atoms1

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