8-Iodo-6-phenylnaphtho[2,1-b]benzofuran CAS 1668553-52-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1668553-52-3
Molecular FormulaC22H13IO
Molecular Weight420.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

8-Iodo-6-phenylnaphtho[2,1-b]benzofuran CAS 1668553-52-3 chemical structure

Description

The molecular framework of 8-Iodo-6-phenylnaphtho[2,1-b]benzofuran (C22H13IO) is characterized by a steroid core, a hydroxyl group, an ether linkage, iodine substitution. 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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

CATO supplies 8-Iodo-6-phenylnaphtho[2,1-b]benzofuran (CAS 1668553-52-3), a certified reference material (molecular formula C22H13IO, MW 420.24 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC22H13IO
Molecular Weight420.24 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
Degree of Unsaturation (DBE)16.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993
Halogen ContentI-containing

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