N-(4-Fluorophenyl)-2H-chromene-3-carboxamide CAS 338420-05-6

Purity 97%+In StockPharmaceutical Standards
CAS No.338420-05-6
Molecular FormulaC16H12FNO2
Molecular Weight269.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-Fluorophenyl)-2H-chromene-3-carboxamide CAS 338420-05-6 chemical structure

Description

N-(4-Fluorophenyl)-2H-chromene-3-carboxamide (CAS 338420-05-6) is a high-purity analytical reference standard with the molecular formula C16H12FNO2 and a molecular weight of 269.27 g/mol.

Based on its molecular formula C16H12FNO2, N-(4-Fluorophenyl)-2H-chromene-3-carboxamide 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 269.27 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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

CATO manufactures N-(4-Fluorophenyl)-2H-chromene-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.

Physical & Chemical Properties

Molecular FormulaC16H12FNO2
Molecular Weight269.27 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF-containing
Nitrogen Atoms1

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