4-(2-fluoro-4-nitrophenoxy)-6,7-dimethoxyquinoline CAS 516526-44-6

Purity 97%+In StockPharmaceutical Standards
CAS No.516526-44-6
Molecular FormulaC17H13FN2O5
Molecular Weight344.29 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(2-fluoro-4-nitrophenoxy)-6,7-dimethoxyquinoline CAS 516526-44-6 chemical structure

Description

CATO supplies 4-(2-fluoro-4-nitrophenoxy)-6,7-dimethoxyquinoline (CAS 516526-44-6), a certified reference material (molecular formula C17H13FN2O5, MW 344.29 g/mol) for analytical method development and quality control.

Based on its molecular formula C17H13FN2O5, 4-(2-fluoro-4-nitrophenoxy)-6,7-dimethoxyquinoline contains a flavonoid core, 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 344.29 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.

CATO manufactures 4-(2-fluoro-4-nitrophenoxy)-6,7-dimethoxyquinoline 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 FormulaC17H13FN2O5
Molecular Weight344.29 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1984
Halogen ContentF-containing
Nitrogen Atoms2

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