Methyl 3-(2-(2-((4-chlorophenyl)amino)-2-oxoacetyl)-1H-pyrrol-1-yl)thiophene-2-carboxylate CAS 477857-80-0

Purity 97%+In StockPharmaceutical Standards
CAS No.477857-80-0
Molecular FormulaC18H13ClN2O4S
Molecular Weight388.82 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 3-(2-(2-((4-chlorophenyl)amino)-2-oxoacetyl)-1H-pyrrol-1-yl)thiophene-2-carboxylate CAS 477857-80-0 chemical structure

Description

CATO supplies Methyl 3-(2-(2-((4-chlorophenyl)amino)-2-oxoacetyl)-1H-pyrrol-1-yl)thiophene-2-carboxylate (CAS 477857-80-0), a certified reference material (molecular formula C18H13ClN2O4S, MW 388.82 g/mol) for analytical method development and quality control.

Owing to a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution, Methyl 3-(2-(2-((4-chlorophenyl)amino)-2-oxoacetyl)-1H-pyrrol-1-yl)thiophene-2-carboxylate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 388.82 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 Methyl 3-(2-(2-((4-chlorophenyl)amino)-2-oxoacetyl)-1H-pyrrol-1-yl)thiophene-2-carboxylate 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 FormulaC18H13ClN2O4S
Molecular Weight388.82 g/mol
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)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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