methyl 4-bromo-3-chloroquinoline-6-carboxylate CAS 1264209-69-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1264209-69-9
Molecular FormulaC11H7BrClNO2
Molecular Weight300.54 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

methyl 4-bromo-3-chloroquinoline-6-carboxylate CAS 1264209-69-9 chemical structure

Description

CATO manufactures methyl 4-bromo-3-chloroquinoline-6-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.

CATO supplies methyl 4-bromo-3-chloroquinoline-6-carboxylate (CAS 1264209-69-9), a certified reference material (molecular formula C11H7BrClNO2, MW 300.54 g/mol) for analytical method development and quality control.

Based on its molecular formula C11H7BrClNO2, methyl 4-bromo-3-chloroquinoline-6-carboxylate contains a nitrogen-containing heterocyclic scaffold, an amide 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 300.54 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 FormulaC11H7BrClNO2
Molecular Weight300.54 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentCl/Br-containing
Nitrogen Atoms1

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