4-Bromophenyl 8-methyl-2-phenylquinoline-4-carboxylate CAS 355421-41-9

Purity 97%+In StockPharmaceutical Standards
CAS No.355421-41-9
Molecular FormulaC23H16BrNO2
Molecular Weight418.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Bromophenyl 8-methyl-2-phenylquinoline-4-carboxylate CAS 355421-41-9 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.

CATO supplies 4-Bromophenyl 8-methyl-2-phenylquinoline-4-carboxylate (CAS 355421-41-9), a certified reference material (molecular formula C23H16BrNO2, MW 418.28 g/mol) for analytical method development and quality control.

Based on its molecular formula C23H16BrNO2, 4-Bromophenyl 8-methyl-2-phenylquinoline-4-carboxylate contains a steroid core, an amide group, a hydroxyl group, an ether linkage, bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 418.28 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO manufactures 4-Bromophenyl 8-methyl-2-phenylquinoline-4-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 FormulaC23H16BrNO2
Molecular Weight418.28 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at room temperature, 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)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentBr-containing
Nitrogen Atoms1

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