N-(1-(2,4-Dichlorophenyl)ethyl)-9-oxo-9H-thioxanthene-3-carboxamide 10,10-dioxide CAS 854040-96-3

Purity 97%+In StockPharmaceutical Standards
CAS No.854040-96-3
Molecular FormulaC22H15Cl2NO4S
Molecular Weight460.33 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(1-(2,4-Dichlorophenyl)ethyl)-9-oxo-9H-thioxanthene-3-carboxamide 10,10-dioxide CAS 854040-96-3 chemical structure

Description

N-(1-(2,4-Dichlorophenyl)ethyl)-9-oxo-9H-thioxanthene-3-carboxamide 10,10-dioxide (CAS 854040-96-3) is a high-purity analytical reference standard with the molecular formula C22H15Cl2NO4S and a molecular weight of 460.33 g/mol.

N-(1-(2,4-Dichlorophenyl)ethyl)-9-oxo-9H-thioxanthene-3-carboxamide 10,10-dioxide (C22H15Cl2NO4S) contains a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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

CATO manufactures N-(1-(2,4-Dichlorophenyl)ethyl)-9-oxo-9H-thioxanthene-3-carboxamide 10,10-dioxide 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 FormulaC22H15Cl2NO4S
Molecular Weight460.33 g/mol
Purity97%+
StorageStore at room temperature, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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