n-(4-Bromo-3-methylphenyl)-2,5-dimethylfuran-3-carboxamide CAS 1016847-22-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1016847-22-5
Molecular FormulaC14H14BrNO2
Molecular Weight308.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

n-(4-Bromo-3-methylphenyl)-2,5-dimethylfuran-3-carboxamide CAS 1016847-22-5 chemical structure

Description

CATO manufactures n-(4-Bromo-3-methylphenyl)-2,5-dimethylfuran-3-carboxamide 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-Bromo-3-methylphenyl)-2,5-dimethylfuran-3-carboxamide (CAS 1016847-22-5) is a high-purity analytical reference standard with the molecular formula C14H14BrNO2 and a molecular weight of 308.17 g/mol.

The molecular framework of n-(4-Bromo-3-methylphenyl)-2,5-dimethylfuran-3-carboxamide (C14H14BrNO2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, bromine 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.

Physical & Chemical Properties

Molecular FormulaC14H14BrNO2
Molecular Weight308.17 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentBr-containing
Nitrogen Atoms1

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