3-(2-Fluoro-4-nitrophenoxy)-N-methyl-N-phenylthiophene-2-carboxamide CAS 303152-51-4

Purity 97%+In StockPharmaceutical Standards
CAS No.303152-51-4
Molecular FormulaC18H13FN2O4S
Molecular Weight372.37 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(2-Fluoro-4-nitrophenoxy)-N-methyl-N-phenylthiophene-2-carboxamide CAS 303152-51-4 chemical structure

Description

Based on its molecular formula C18H13FN2O4S, 3-(2-Fluoro-4-nitrophenoxy)-N-methyl-N-phenylthiophene-2-carboxamide contains a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 372.37 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.

3-(2-Fluoro-4-nitrophenoxy)-N-methyl-N-phenylthiophene-2-carboxamide (CAS 303152-51-4) is a high-purity analytical reference standard with the molecular formula C18H13FN2O4S and a molecular weight of 372.37 g/mol.

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 3-(2-Fluoro-4-nitrophenoxy)-N-methyl-N-phenylthiophene-2-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.

Physical & Chemical Properties

Molecular FormulaC18H13FN2O4S
Molecular Weight372.37 g/mol
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)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms1

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