2-(4-Bromophenyl)-6-methylquinoline-4-carboxylic acid CAS 351332-55-3

Purity 97%+In StockPharmaceutical Standards
CAS No.351332-55-3
Molecular FormulaC17H12BrNO2
Molecular Weight342.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(4-Bromophenyl)-6-methylquinoline-4-carboxylic acid CAS 351332-55-3 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

2-(4-Bromophenyl)-6-methylquinoline-4-carboxylic acid (CAS 351332-55-3), molecular formula C17H12BrNO2 and molecular weight 342.19 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C17H12BrNO2, 2-(4-Bromophenyl)-6-methylquinoline-4-carboxylic acid 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 342.19 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.

CATO manufactures 2-(4-Bromophenyl)-6-methylquinoline-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.

Physical & Chemical Properties

Molecular FormulaC17H12BrNO2
Molecular Weight342.19 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.)2025
Halogen ContentBr-containing
Nitrogen Atoms1

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