2,6-Bis(benzyloxy)-3-(4-iodophenyl)pyridine CAS 2758531-28-9

Purity 97%+In StockPharmaceutical Standards
CAS No.2758531-28-9
Molecular FormulaC25H20INO2
Molecular Weight493.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,6-Bis(benzyloxy)-3-(4-iodophenyl)pyridine CAS 2758531-28-9 chemical structure

Description

The occurrence of 2,6-Bis(benzyloxy)-3-(4-iodophenyl)pyridine is closely related to a steroid core, an amide group, a hydroxyl group, an ether linkage, iodine substitution in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 2,6-Bis(benzyloxy)-3-(4-iodophenyl)pyridine (CAS 2758531-28-9), a certified reference material (molecular formula C25H20INO2, MW 493.34 g/mol) for analytical method development and quality control.

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, iodine substitution, 2,6-Bis(benzyloxy)-3-(4-iodophenyl)pyridine is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 493.34 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

CATO manufactures 2,6-Bis(benzyloxy)-3-(4-iodophenyl)pyridine 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 FormulaC25H20INO2
Molecular Weight493.34 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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.)2002
Halogen ContentI-containing
Nitrogen Atoms1

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