2-(Pyridin-3-yl)-5-(p-tolyl)-1,3,4-oxadiazole CAS 56352-92-2

Purity 97%+In StockPharmaceutical Standards
CAS No.56352-92-2
Molecular FormulaC14H11N3O
Molecular Weight237.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(Pyridin-3-yl)-5-(p-tolyl)-1,3,4-oxadiazole CAS 56352-92-2 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 2-(Pyridin-3-yl)-5-(p-tolyl)-1,3,4-oxadiazole.

CATO supplies 2-(Pyridin-3-yl)-5-(p-tolyl)-1,3,4-oxadiazole (CAS 56352-92-2), a certified reference material (molecular formula C14H11N3O, MW 237.26 g/mol) for analytical method development and quality control.

The molecular framework of 2-(Pyridin-3-yl)-5-(p-tolyl)-1,3,4-oxadiazole (C14H11N3O) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC14H11N3O
Molecular Weight237.26 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1973
Nitrogen Atoms3

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