N-(5-(benzyloxy)-2,4-dichlorophenyl)-3-(4-nitrophenoxy)thiophene-2-carboxamide CAS 339015-27-9

Purity 97%+In StockPharmaceutical Standards
CAS No.339015-27-9
Molecular FormulaC24H16Cl2N2O5S
Molecular Weight515.37 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(5-(benzyloxy)-2,4-dichlorophenyl)-3-(4-nitrophenoxy)thiophene-2-carboxamide CAS 339015-27-9 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.

N-(5-(benzyloxy)-2,4-dichlorophenyl)-3-(4-nitrophenoxy)thiophene-2-carboxamide (CAS 339015-27-9) is a high-purity analytical reference standard with the molecular formula C24H16Cl2N2O5S and a molecular weight of 515.37 g/mol.

N-(5-(benzyloxy)-2,4-dichlorophenyl)-3-(4-nitrophenoxy)thiophene-2-carboxamide (C24H16Cl2N2O5S) contains a flavonoid core, an amide group, a sulfone 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO manufactures N-(5-(benzyloxy)-2,4-dichlorophenyl)-3-(4-nitrophenoxy)thiophene-2-carboxamide 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.

Physical & Chemical Properties

Molecular FormulaC24H16Cl2N2O5S
Molecular Weight515.37 g/mol
Purity97%+
StorageStore in a cool place (≤25°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)17.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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