Ethyl 5-(4-bromophenyl)-2-phenyl-1H-pyrrole-3-carboxylate CAS 65473-91-8

Purity 97%+In StockPharmaceutical Standards
CAS No.65473-91-8
Molecular FormulaC19H16BrNO2
Molecular Weight370.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Ethyl 5-(4-bromophenyl)-2-phenyl-1H-pyrrole-3-carboxylate CAS 65473-91-8 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.

CATO supplies Ethyl 5-(4-bromophenyl)-2-phenyl-1H-pyrrole-3-carboxylate (CAS 65473-91-8), a certified reference material (molecular formula C19H16BrNO2, MW 370.24 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, bromine substitution, Ethyl 5-(4-bromophenyl)-2-phenyl-1H-pyrrole-3-carboxylate is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 370.24 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).

CATO manufactures Ethyl 5-(4-bromophenyl)-2-phenyl-1H-pyrrole-3-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 FormulaC19H16BrNO2
Molecular Weight370.24 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 chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1975
Halogen ContentBr-containing
Nitrogen Atoms1

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