3-(4-(tert-Butyl)phenyl)-5-(2-chloropyridin-4-yl)-1,2,4-oxadiazole CAS 1119396-18-7

Purity 97%+In StockPharmaceutical Standards
CAS No.1119396-18-7
Molecular FormulaC17H16ClN3O
Molecular Weight313.78 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(4-(tert-Butyl)phenyl)-5-(2-chloropyridin-4-yl)-1,2,4-oxadiazole CAS 1119396-18-7 chemical structure

Description

CATO manufactures 3-(4-(tert-Butyl)phenyl)-5-(2-chloropyridin-4-yl)-1,2,4-oxadiazole under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

3-(4-(tert-Butyl)phenyl)-5-(2-chloropyridin-4-yl)-1,2,4-oxadiazole (CAS 1119396-18-7), molecular formula C17H16ClN3O and molecular weight 313.78 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 3-(4-(tert-Butyl)phenyl)-5-(2-chloropyridin-4-yl)-1,2,4-oxadiazole (C17H16ClN3O) is characterized by a steroid core, 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. 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.

Physical & Chemical Properties

Molecular FormulaC17H16ClN3O
Molecular Weight313.78 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
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.)1989
Halogen ContentCl-containing
Nitrogen Atoms3

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