N-(3-bromophenyl)-4-((2-chlorothiazol-5-yl)methoxy)benzenesulfonamide CAS 339105-51-0

Purity 97%+In StockPharmaceutical Standards
CAS No.339105-51-0
Molecular FormulaC16H12BrClN2O3S2
Molecular Weight459.77 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(3-bromophenyl)-4-((2-chlorothiazol-5-yl)methoxy)benzenesulfonamide CAS 339105-51-0 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.

N-(3-bromophenyl)-4-((2-chlorothiazol-5-yl)methoxy)benzenesulfonamide (CAS 339105-51-0) is a high-purity analytical reference standard with the molecular formula C16H12BrClN2O3S2 and a molecular weight of 459.77 g/mol.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine/bromine substitution, N-(3-bromophenyl)-4-((2-chlorothiazol-5-yl)methoxy)benzenesulfonamide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 459.77 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO manufactures N-(3-bromophenyl)-4-((2-chlorothiazol-5-yl)methoxy)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 FormulaC16H12BrClN2O3S2
Molecular Weight459.77 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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl/Br-containing
Nitrogen Atoms2
Sulfur Atoms2

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