4-Bromo-2-fluoro-N-(4-methylthiazol-2-yl)benzenesulfonamide CAS 1771023-86-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1771023-86-9
Molecular FormulaC10H8BrFN2O2S2
Molecular Weight351.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Bromo-2-fluoro-N-(4-methylthiazol-2-yl)benzenesulfonamide CAS 1771023-86-9 chemical structure

Description

CATO manufactures 4-Bromo-2-fluoro-N-(4-methylthiazol-2-yl)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.

4-Bromo-2-fluoro-N-(4-methylthiazol-2-yl)benzenesulfonamide (CAS 1771023-86-9) is a high-purity analytical reference standard with the molecular formula C10H8BrFN2O2S2 and a molecular weight of 351.22 g/mol.

Structurally, 4-Bromo-2-fluoro-N-(4-methylthiazol-2-yl)benzenesulfonamide (C10H8BrFN2O2S2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine/bromine substitution. The molecule exhibits a degree of unsaturation (DBE) of 7.0, corresponding to approximately 7 ring(s) or double-bond equivalent(s). With a molecular weight of 351.22 g/mol, it falls into the moderately-high-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 FormulaC10H8BrFN2O2S2
Molecular Weight351.22 g/mol
Purity97%+
StorageStore at 2-8°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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1994
Halogen ContentF/Br-containing
Nitrogen Atoms2
Sulfur Atoms2

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