(5-Fluorobenzo[d]isoxazol-3-yl)methanesulfonamide CAS 68291-99-6

Purity 97%+In StockPharmaceutical Standards
CAS No.68291-99-6
Molecular FormulaC8H7FN2O3S
Molecular Weight230.22 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(5-Fluorobenzo[d]isoxazol-3-yl)methanesulfonamide CAS 68291-99-6 chemical structure

Description

CATO manufactures (5-Fluorobenzo[d]isoxazol-3-yl)methanesulfonamide 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.

(5-Fluorobenzo[d]isoxazol-3-yl)methanesulfonamide (CAS 68291-99-6) is a high-purity analytical reference standard with the molecular formula C8H7FN2O3S and a molecular weight of 230.22 g/mol.

(5-Fluorobenzo[d]isoxazol-3-yl)methanesulfonamide (C8H7FN2O3S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

Physical & Chemical Properties

Molecular FormulaC8H7FN2O3S
Molecular Weight230.22 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO
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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1976
Halogen ContentF-containing
Nitrogen Atoms2
Sulfur Atoms1

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