2-(4-Bromophenyl)-8-chloroquinoline-4-carbonyl chloride CAS 1160263-61-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1160263-61-5
Molecular FormulaC16H8BrCl2NO
Molecular Weight381.05 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(4-Bromophenyl)-8-chloroquinoline-4-carbonyl chloride CAS 1160263-61-5 chemical structure

Description

Based on its molecular formula C16H8BrCl2NO, 2-(4-Bromophenyl)-8-chloroquinoline-4-carbonyl chloride 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 381.05 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.

CATO supplies 2-(4-Bromophenyl)-8-chloroquinoline-4-carbonyl chloride (CAS 1160263-61-5), a certified reference material (molecular formula C16H8BrCl2NO, MW 381.05 g/mol) for analytical method development and quality control.

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.

CATO manufactures 2-(4-Bromophenyl)-8-chloroquinoline-4-carbonyl chloride 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 FormulaC16H8BrCl2NO
Molecular Weight381.05 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
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentCl/Br-containing
Nitrogen Atoms1

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