3-[(4-Bromophenyl)sulfanyl]-2-phenylquinoline-4-carboxylic acid CAS 477886-46-7

Purity 97%+In StockPharmaceutical Standards
CAS No.477886-46-7
Molecular FormulaC22H14BrNO2S
Molecular Weight436.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-[(4-Bromophenyl)sulfanyl]-2-phenylquinoline-4-carboxylic acid CAS 477886-46-7 chemical structure

Description

CATO manufactures 3-[(4-Bromophenyl)sulfanyl]-2-phenylquinoline-4-carboxylic acid 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.

CATO supplies 3-[(4-Bromophenyl)sulfanyl]-2-phenylquinoline-4-carboxylic acid (CAS 477886-46-7), a certified reference material (molecular formula C22H14BrNO2S, MW 436.32 g/mol) for analytical method development and quality control.

Based on its molecular formula C22H14BrNO2S, 3-[(4-Bromophenyl)sulfanyl]-2-phenylquinoline-4-carboxylic acid contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 436.32 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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.

Physical & Chemical Properties

Molecular FormulaC22H14BrNO2S
Molecular Weight436.32 g/mol
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
Sulfur Atoms1

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