N-(4-Chloro-2-methylphenyl)-4-methoxybenzamide CAS 349089-38-9

Purity 97%+In StockPharmaceutical Standards
CAS No.349089-38-9
Molecular FormulaC15H14ClNO2
Molecular Weight275.73 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-Chloro-2-methylphenyl)-4-methoxybenzamide CAS 349089-38-9 chemical structure

Description

N-(4-Chloro-2-methylphenyl)-4-methoxybenzamide (CAS 349089-38-9) is a high-purity analytical reference standard with the molecular formula C15H14ClNO2 and a molecular weight of 275.73 g/mol.

The molecular framework of N-(4-Chloro-2-methylphenyl)-4-methoxybenzamide (C15H14ClNO2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, chlorine 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

CATO manufactures N-(4-Chloro-2-methylphenyl)-4-methoxybenzamide 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 FormulaC15H14ClNO2
Molecular Weight275.73 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms1

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