Ethyl 3-(1-(3,4-dimethoxyphenyl)-5-oxopyrrolidine-3-carboxamido)benzoate CAS 1291842-44-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1291842-44-8
Molecular FormulaC22H24N2O6
Molecular Weight412.44 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 3-(1-(3,4-dimethoxyphenyl)-5-oxopyrrolidine-3-carboxamido)benzoate CAS 1291842-44-8 chemical structure

Description

The molecular framework of Ethyl 3-(1-(3,4-dimethoxyphenyl)-5-oxopyrrolidine-3-carboxamido)benzoate (C22H24N2O6) is characterized by a flavonoid core, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

Ethyl 3-(1-(3,4-dimethoxyphenyl)-5-oxopyrrolidine-3-carboxamido)benzoate (CAS 1291842-44-8) is a high-purity analytical reference standard with the molecular formula C22H24N2O6 and a molecular weight of 412.44 g/mol.

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 manufactures Ethyl 3-(1-(3,4-dimethoxyphenyl)-5-oxopyrrolidine-3-carboxamido)benzoate 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 FormulaC22H24N2O6
Molecular Weight412.44 g/mol
AppearancePale yellow to yellow crystalline powder
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
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms2

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