2-Chloro-4-fluoro-5-iodophenyl trifluoromethanesulfonate CAS 1820607-92-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1820607-92-8
Molecular FormulaC7H2ClF4IO3S
Molecular Weight404.51 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Chloro-4-fluoro-5-iodophenyl trifluoromethanesulfonate CAS 1820607-92-8 chemical structure

Description

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 supplies 2-Chloro-4-fluoro-5-iodophenyl trifluoromethanesulfonate (CAS 1820607-92-8), a certified reference material (molecular formula C7H2ClF4IO3S, MW 404.51 g/mol) for analytical method development and quality control.

The molecular framework of 2-Chloro-4-fluoro-5-iodophenyl trifluoromethanesulfonate (C7H2ClF4IO3S) is characterized by a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine/chlorine/iodine substitution, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional groups, 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.

CATO manufactures 2-Chloro-4-fluoro-5-iodophenyl trifluoromethanesulfonate 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 FormulaC7H2ClF4IO3S
Molecular Weight404.51 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO, water
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.)1995
Halogen ContentF/Cl/I-containing
Sulfur Atoms1

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