N-(4-Bromophenyl)-2-((4-((2-hydroxybenzylidene)amino)phenyl)thio)acetamide CAS 765285-03-8

Purity 97%+In StockPharmaceutical Standards
CAS No.765285-03-8
Molecular FormulaC21H17BrN2O2S
Molecular Weight441.34 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-Bromophenyl)-2-((4-((2-hydroxybenzylidene)amino)phenyl)thio)acetamide CAS 765285-03-8 chemical structure

Description

CATO manufactures N-(4-Bromophenyl)-2-((4-((2-hydroxybenzylidene)amino)phenyl)thio)acetamide 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.

N-(4-Bromophenyl)-2-((4-((2-hydroxybenzylidene)amino)phenyl)thio)acetamide (CAS 765285-03-8), molecular formula C21H17BrN2O2S and molecular weight 441.34 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C21H17BrN2O2S, N-(4-Bromophenyl)-2-((4-((2-hydroxybenzylidene)amino)phenyl)thio)acetamide contains a steroid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, bromine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 441.34 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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.

Physical & Chemical Properties

Molecular FormulaC21H17BrN2O2S
Molecular Weight441.34 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; 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.)1986
Halogen ContentBr-containing
Nitrogen Atoms2
Sulfur Atoms1

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