1-(2-Fluorophenyl)-2-tosylethanone CAS 1492822-28-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1492822-28-2
Molecular FormulaC15H13FO3S
Molecular Weight292.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(2-Fluorophenyl)-2-tosylethanone CAS 1492822-28-2 chemical structure

Description

1-(2-Fluorophenyl)-2-tosylethanone (CAS 1492822-28-2) is a high-purity analytical reference standard with the molecular formula C15H13FO3S and a molecular weight of 292.33 g/mol.

Based on its molecular formula C15H13FO3S, 1-(2-Fluorophenyl)-2-tosylethanone contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution, a polycyclic aromatic system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 292.33 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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 1-(2-Fluorophenyl)-2-tosylethanone 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 FormulaC15H13FO3S
Molecular Weight292.33 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentF-containing
Sulfur Atoms1

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