2,6-Dibromo-3-(2-(2,4-dichlorophenoxy)ethoxy)pyridine CAS 1355026-47-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1355026-47-9
Molecular FormulaC13H9Br2Cl2NO2
Molecular Weight441.93 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,6-Dibromo-3-(2-(2,4-dichlorophenoxy)ethoxy)pyridine CAS 1355026-47-9 chemical structure

Description

Structurally, 2,6-Dibromo-3-(2-(2,4-dichlorophenoxy)ethoxy)pyridine (C13H9Br2Cl2NO2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine/bromine substitution. The molecule exhibits a degree of unsaturation (DBE) of 8.0, corresponding to approximately 8 ring(s) or double-bond equivalent(s). With a molecular weight of 441.93 g/mol, it falls into the moderately-high-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

2,6-Dibromo-3-(2-(2,4-dichlorophenoxy)ethoxy)pyridine (CAS 1355026-47-9), molecular formula C13H9Br2Cl2NO2 and molecular weight 441.93 g/mol, is a CATO reference standard with documented purity and traceability.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), 2,6-Dibromo-3-(2-(2,4-dichlorophenoxy)ethoxy)pyridine 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 FormulaC13H9Br2Cl2NO2
Molecular Weight441.93 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl/Br-containing
Nitrogen Atoms1

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