4-Chlorophenyl 2-(4-bromophenyl)quinoline-4-carboxylate CAS 355433-73-7

Purity 97%+In StockPharmaceutical Standards
CAS No.355433-73-7
Molecular FormulaC22H13BrClNO2
Molecular Weight438.70 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Chlorophenyl 2-(4-bromophenyl)quinoline-4-carboxylate CAS 355433-73-7 chemical structure

Description

Structurally, 4-Chlorophenyl 2-(4-bromophenyl)quinoline-4-carboxylate (C22H13BrClNO2) contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine/bromine substitution. The molecule exhibits a degree of unsaturation (DBE) of 16.0, corresponding to approximately 16 ring(s) or double-bond equivalent(s). With a molecular weight of 438.70 g/mol, it falls into the moderately-high-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

4-Chlorophenyl 2-(4-bromophenyl)quinoline-4-carboxylate (CAS 355433-73-7) is a high-purity analytical reference standard with the molecular formula C22H13BrClNO2 and a molecular weight of 438.70 g/mol.

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 4-Chlorophenyl 2-(4-bromophenyl)quinoline-4-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.

Physical & Chemical Properties

Molecular FormulaC22H13BrClNO2
Molecular Weight438.70 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at room temperature, 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)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl/Br-containing
Nitrogen Atoms1

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