2-(3-Bromophenyl)-8-methylquinoline-4-carboxylic acid CAS 438229-60-8

Purity 97%+In StockPharmaceutical Standards
CAS No.438229-60-8
Molecular FormulaC17H12BrNO2
Molecular Weight342.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(3-Bromophenyl)-8-methylquinoline-4-carboxylic acid CAS 438229-60-8 chemical structure

Description

CATO manufactures 2-(3-Bromophenyl)-8-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.

2-(3-Bromophenyl)-8-methylquinoline-4-carboxylic acid (CAS 438229-60-8) is a high-purity analytical reference standard with the molecular formula C17H12BrNO2 and a molecular weight of 342.19 g/mol.

The molecular framework of 2-(3-Bromophenyl)-8-methylquinoline-4-carboxylic acid (C17H12BrNO2) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage, bromine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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