N-(4-((4-Fluorobenzamido)methyl)phenyl)-N-methylbenzamide CAS 1956389-97-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1956389-97-1
Molecular FormulaC22H19FN2O2
Molecular Weight362.40 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-((4-Fluorobenzamido)methyl)phenyl)-N-methylbenzamide CAS 1956389-97-1 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

CATO supplies N-(4-((4-Fluorobenzamido)methyl)phenyl)-N-methylbenzamide (CAS 1956389-97-1), a certified reference material (molecular formula C22H19FN2O2, MW 362.40 g/mol) for analytical method development and quality control.

The molecular framework of N-(4-((4-Fluorobenzamido)methyl)phenyl)-N-methylbenzamide (C22H19FN2O2) is characterized by a steroid core, an amide group, a hydroxyl group, an ether linkage, fluorine 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 aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO manufactures N-(4-((4-Fluorobenzamido)methyl)phenyl)-N-methylbenzamide 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 FormulaC22H19FN2O2
Molecular Weight362.40 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°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.)1996
Halogen ContentF-containing
Nitrogen Atoms2

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