3-[(1,1-Dioxido-1,2-benzisothiazol-3-yl)amino]phenyl 2-chloroacetate CAS 958697-63-7

Purity 97%+In StockPharmaceutical Standards
CAS No.958697-63-7
Molecular FormulaC15H11ClN2O4S
Molecular Weight350.78 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-[(1,1-Dioxido-1,2-benzisothiazol-3-yl)amino]phenyl 2-chloroacetate CAS 958697-63-7 chemical structure

Description

CATO supplies 3-[(1,1-Dioxido-1,2-benzisothiazol-3-yl)amino]phenyl 2-chloroacetate (CAS 958697-63-7), a certified reference material (molecular formula C15H11ClN2O4S, MW 350.78 g/mol) for analytical method development and quality control.

Based on its molecular formula C15H11ClN2O4S, 3-[(1,1-Dioxido-1,2-benzisothiazol-3-yl)amino]phenyl 2-chloroacetate 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 350.78 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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.

CATO manufactures 3-[(1,1-Dioxido-1,2-benzisothiazol-3-yl)amino]phenyl 2-chloroacetate 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 FormulaC15H11ClN2O4S
Molecular Weight350.78 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)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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