Ethyl 3-(3,4-dichlorophenyl)-[1,2,4]oxadiazole-5-carboxylate CAS 1053656-34-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1053656-34-0
Molecular FormulaC11H8Cl2N2O3
Molecular Weight287.10 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 3-(3,4-dichlorophenyl)-[1,2,4]oxadiazole-5-carboxylate CAS 1053656-34-0 chemical structure

Description

Ethyl 3-(3,4-dichlorophenyl)-[1,2,4]oxadiazole-5-carboxylate (C11H8Cl2N2O3) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies Ethyl 3-(3,4-dichlorophenyl)-[1,2,4]oxadiazole-5-carboxylate (CAS 1053656-34-0), a certified reference material (molecular formula C11H8Cl2N2O3, MW 287.10 g/mol) for analytical method development and quality control.

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), Ethyl 3-(3,4-dichlorophenyl)-[1,2,4]oxadiazole-5-carboxylate 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 FormulaC11H8Cl2N2O3
Molecular Weight287.10 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, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentCl-containing
Nitrogen Atoms2

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