1-((4-Fluorophenyl)thio)-3-methoxypropan-2-one CAS 1513400-99-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1513400-99-1
Molecular FormulaC10H11FO2S
Molecular Weight214.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-((4-Fluorophenyl)thio)-3-methoxypropan-2-one CAS 1513400-99-1 chemical structure

Description

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.

CATO supplies 1-((4-Fluorophenyl)thio)-3-methoxypropan-2-one (CAS 1513400-99-1), a certified reference material (molecular formula C10H11FO2S, MW 214.26 g/mol) for analytical method development and quality control.

1-((4-Fluorophenyl)thio)-3-methoxypropan-2-one (C10H11FO2S) contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC10H11FO2S
Molecular Weight214.26 g/mol
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentF-containing
Sulfur Atoms1

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