2-[(4-Methylphenyl)formamido]-3-phenylprop-2-enoic acid CAS 109448-26-2

Purity 97%+In StockPharmaceutical Standards
CAS No.109448-26-2
Molecular FormulaC17H15NO3
Molecular Weight281.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-[(4-Methylphenyl)formamido]-3-phenylprop-2-enoic acid CAS 109448-26-2 chemical structure

Description

CATO manufactures 2-[(4-Methylphenyl)formamido]-3-phenylprop-2-enoic 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 2-[(4-Methylphenyl)formamido]-3-phenylprop-2-enoic acid (CAS 109448-26-2), a certified reference material (molecular formula C17H15NO3, MW 281.31 g/mol) for analytical method development and quality control.

2-[(4-Methylphenyl)formamido]-3-phenylprop-2-enoic acid (C17H15NO3) contains a steroid core, an amide group, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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 FormulaC17H15NO3
Molecular Weight281.31 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Nitrogen Atoms1

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