5-Bromo-2-((2-chlorobenzyl)oxy)-3-iodobenzaldehyde CAS 832674-04-1

Purity 97%+In StockPharmaceutical Standards
CAS No.832674-04-1
Molecular FormulaC14H9BrClIO2
Molecular Weight451.48 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-Bromo-2-((2-chlorobenzyl)oxy)-3-iodobenzaldehyde CAS 832674-04-1 chemical structure

Description

The molecular framework of 5-Bromo-2-((2-chlorobenzyl)oxy)-3-iodobenzaldehyde (C14H9BrClIO2) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine/bromine/iodine substitution, a polycyclic aromatic system. 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies 5-Bromo-2-((2-chlorobenzyl)oxy)-3-iodobenzaldehyde (CAS 832674-04-1), a certified reference material (molecular formula C14H9BrClIO2, MW 451.48 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 5-Bromo-2-((2-chlorobenzyl)oxy)-3-iodobenzaldehyde 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 FormulaC14H9BrClIO2
Molecular Weight451.48 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentCl/Br/I-containing

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