2-((4-(Difluoromethoxy)-3-methoxybenzyl)thio)acetic acid CAS 923149-01-3

Purity 97%+In StockPharmaceutical Standards
CAS No.923149-01-3
Molecular FormulaC11H12F2O4S
Molecular Weight278.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-((4-(Difluoromethoxy)-3-methoxybenzyl)thio)acetic acid CAS 923149-01-3 chemical structure

Description

2-((4-(Difluoromethoxy)-3-methoxybenzyl)thio)acetic acid (CAS 923149-01-3), molecular formula C11H12F2O4S and molecular weight 278.27 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 2-((4-(Difluoromethoxy)-3-methoxybenzyl)thio)acetic acid (C11H12F2O4S) is characterized by a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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.

CATO manufactures 2-((4-(Difluoromethoxy)-3-methoxybenzyl)thio)acetic acid 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 FormulaC11H12F2O4S
Molecular Weight278.27 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentF-containing
Sulfur Atoms1

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