6-Fluoro-3-iodo-7-methoxy-2-methylquinolin-4(1h)-one CAS 1599467-53-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1599467-53-4
Molecular FormulaC11H9FINO2
Molecular Weight333.10 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

6-Fluoro-3-iodo-7-methoxy-2-methylquinolin-4(1h)-one CAS 1599467-53-4 chemical structure

Description

Based on its molecular formula C11H9FINO2, 6-Fluoro-3-iodo-7-methoxy-2-methylquinolin-4(1h)-one contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine/iodine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 333.10 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

6-Fluoro-3-iodo-7-methoxy-2-methylquinolin-4(1h)-one (CAS 1599467-53-4) is a high-purity analytical reference standard with the molecular formula C11H9FINO2 and a molecular weight of 333.10 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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC11H9FINO2
Molecular Weight333.10 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993
Halogen ContentF/I-containing
Nitrogen Atoms1

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