3-((4-Bromophenyl)amino)-2-(3,4-dimethoxyphenyl)-1H-inden-1-one CAS 1024337-22-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1024337-22-1
Molecular FormulaC23H18BrNO3
Molecular Weight436.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-((4-Bromophenyl)amino)-2-(3,4-dimethoxyphenyl)-1H-inden-1-one CAS 1024337-22-1 chemical structure

Description

Owing to a steroid core, an amide group, a hydroxyl group, an ether linkage, bromine substitution, 3-((4-Bromophenyl)amino)-2-(3,4-dimethoxyphenyl)-1H-inden-1-one is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 436.30 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).

3-((4-Bromophenyl)amino)-2-(3,4-dimethoxyphenyl)-1H-inden-1-one (CAS 1024337-22-1) is a high-purity analytical reference standard with the molecular formula C23H18BrNO3 and a molecular weight of 436.30 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.

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 FormulaC23H18BrNO3
Molecular Weight436.30 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
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)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentBr-containing
Nitrogen Atoms1

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