6-bromo-2-(5-chlorothiophen-2-yl)-8-methylquinoline-4-carboxylic acid CAS 1405749-71-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1405749-71-4
Molecular FormulaC15H9BrClNO2S
Molecular Weight382.66 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-bromo-2-(5-chlorothiophen-2-yl)-8-methylquinoline-4-carboxylic acid CAS 1405749-71-4 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.

6-bromo-2-(5-chlorothiophen-2-yl)-8-methylquinoline-4-carboxylic acid (CAS 1405749-71-4), molecular formula C15H9BrClNO2S and molecular weight 382.66 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C15H9BrClNO2S, 6-bromo-2-(5-chlorothiophen-2-yl)-8-methylquinoline-4-carboxylic acid contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine/bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 382.66 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.

As a certified reference material (CRM), 6-bromo-2-(5-chlorothiophen-2-yl)-8-methylquinoline-4-carboxylic acid meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC15H9BrClNO2S
Molecular Weight382.66 g/mol
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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl/Br-containing
Nitrogen Atoms1
Sulfur Atoms1

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