4-Chloro-N-(2-(4-((4-chlorophenyl)sulfonyl)piperazin-1-yl)ethyl)benzenesulfonamide CAS 547733-50-6

Purity 97%+In StockPharmaceutical Standards
CAS No.547733-50-6
Molecular FormulaC18H21Cl2N3O4S2
Molecular Weight478.41 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Chloro-N-(2-(4-((4-chlorophenyl)sulfonyl)piperazin-1-yl)ethyl)benzenesulfonamide CAS 547733-50-6 chemical structure

Description

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

4-Chloro-N-(2-(4-((4-chlorophenyl)sulfonyl)piperazin-1-yl)ethyl)benzenesulfonamide (CAS 547733-50-6), molecular formula C18H21Cl2N3O4S2 and molecular weight 478.41 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C18H21Cl2N3O4S2, 4-Chloro-N-(2-(4-((4-chlorophenyl)sulfonyl)piperazin-1-yl)ethyl)benzenesulfonamide contains a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 478.41 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO manufactures 4-Chloro-N-(2-(4-((4-chlorophenyl)sulfonyl)piperazin-1-yl)ethyl)benzenesulfonamide 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 FormulaC18H21Cl2N3O4S2
Molecular Weight478.41 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; 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.)1984
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms2

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