(2E)-3-{4-[(4-bromophenyl)methoxy]phenyl}-N-[(4-methylphenyl)methyl]prop-2-enamide CAS 477889-36-4

Purity 97%+In StockPharmaceutical Standards
CAS No.477889-36-4
Molecular FormulaC24H22BrNO2
Molecular Weight436.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(2E)-3-{4-[(4-bromophenyl)methoxy]phenyl}-N-[(4-methylphenyl)methyl]prop-2-enamide CAS 477889-36-4 chemical structure

Description

(2E)-3-{4-[(4-bromophenyl)methoxy]phenyl}-N-[(4-methylphenyl)methyl]prop-2-enamide (CAS 477889-36-4) is a high-purity analytical reference standard with the molecular formula C24H22BrNO2 and a molecular weight of 436.34 g/mol.

The molecular framework of (2E)-3-{4-[(4-bromophenyl)methoxy]phenyl}-N-[(4-methylphenyl)methyl]prop-2-enamide (C24H22BrNO2) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage, bromine 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 (2E)-3-{4-[(4-bromophenyl)methoxy]phenyl}-N-[(4-methylphenyl)methyl]prop-2-enamide 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 FormulaC24H22BrNO2
Molecular Weight436.34 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)14.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentBr-containing
Nitrogen Atoms1

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