4-(3-Chloro-1-adamantyl)benzenesulfonyl chloride CAS 1354356-42-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1354356-42-5
Molecular FormulaC16H18Cl2O2S
Molecular Weight345.28 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(3-Chloro-1-adamantyl)benzenesulfonyl chloride CAS 1354356-42-5 chemical structure

Description

CATO manufactures 4-(3-Chloro-1-adamantyl)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.

CATO supplies 4-(3-Chloro-1-adamantyl)benzenesulfonyl chloride (CAS 1354356-42-5), a certified reference material (molecular formula C16H18Cl2O2S, MW 345.28 g/mol) for analytical method development and quality control.

4-(3-Chloro-1-adamantyl)benzenesulfonyl chloride (C16H18Cl2O2S) contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution, a polycyclic aromatic 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. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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 FormulaC16H18Cl2O2S
Molecular Weight345.28 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1991
Halogen ContentCl-containing
Sulfur Atoms1

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