3-((2,4-Dichlorophenoxy)methyl)-5-phenyl-1,2,4-oxadiazole CAS 4780-17-0

Purity 97%+In StockPharmaceutical Standards
CAS No.4780-17-0
Molecular FormulaC15H10Cl2N2O2
Molecular Weight321.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-((2,4-Dichlorophenoxy)methyl)-5-phenyl-1,2,4-oxadiazole CAS 4780-17-0 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-((2,4-Dichlorophenoxy)methyl)-5-phenyl-1,2,4-oxadiazole (CAS 4780-17-0), a certified reference material (molecular formula C15H10Cl2N2O2, MW 321.16 g/mol) for analytical method development and quality control.

The molecular framework of 3-((2,4-Dichlorophenoxy)methyl)-5-phenyl-1,2,4-oxadiazole (C15H10Cl2N2O2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

As a certified reference material (CRM), 3-((2,4-Dichlorophenoxy)methyl)-5-phenyl-1,2,4-oxadiazole 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 FormulaC15H10Cl2N2O2
Molecular Weight321.16 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958
Halogen ContentCl-containing
Nitrogen Atoms2

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