4-(Benzyl(methyl)amino)-3,5-difluorobenzoic acid CAS 1404196-20-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1404196-20-8
Molecular FormulaC15H13F2NO2
Molecular Weight277.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(Benzyl(methyl)amino)-3,5-difluorobenzoic acid CAS 1404196-20-8 chemical structure

Description

CATO manufactures 4-(Benzyl(methyl)amino)-3,5-difluorobenzoic acid 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.

CATO supplies 4-(Benzyl(methyl)amino)-3,5-difluorobenzoic acid (CAS 1404196-20-8), a certified reference material (molecular formula C15H13F2NO2, MW 277.27 g/mol) for analytical method development and quality control.

Based on its molecular formula C15H13F2NO2, 4-(Benzyl(methyl)amino)-3,5-difluorobenzoic acid contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 277.27 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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

Physical & Chemical Properties

Molecular FormulaC15H13F2NO2
Molecular Weight277.27 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
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.)1991
Halogen ContentF-containing
Nitrogen Atoms1

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