4-Methoxy-3-(trifluoromethoxy)benzenesulfonyl chloride CAS 956468-19-2

Purity 97%+In StockPharmaceutical Standards
CAS No.956468-19-2
Molecular FormulaC8H6ClF3O4S
Molecular Weight290.64 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Methoxy-3-(trifluoromethoxy)benzenesulfonyl chloride CAS 956468-19-2 chemical structure

Description

Structurally, 4-Methoxy-3-(trifluoromethoxy)benzenesulfonyl chloride (C8H6ClF3O4S) contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution, an aromatic ring system. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 290.64 g/mol, it falls into the medium-molecular-weight range. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO supplies 4-Methoxy-3-(trifluoromethoxy)benzenesulfonyl chloride (CAS 956468-19-2), a certified reference material (molecular formula C8H6ClF3O4S, MW 290.64 g/mol) for analytical method development and quality control.

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 4-Methoxy-3-(trifluoromethoxy)benzenesulfonyl chloride 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 FormulaC8H6ClF3O4S
Molecular Weight290.64 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF/Cl-containing
Sulfur Atoms1

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