N-(4-chloro-3-nitrophenyl)-2-((4-chlorophenyl)thio)acetamide CAS 197512-96-2

Purity 97%+In StockPharmaceutical Standards
CAS No.197512-96-2
Molecular FormulaC14H10Cl2N2O3S
Molecular Weight357.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-chloro-3-nitrophenyl)-2-((4-chlorophenyl)thio)acetamide CAS 197512-96-2 chemical structure

Description

CATO manufactures N-(4-chloro-3-nitrophenyl)-2-((4-chlorophenyl)thio)acetamide 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.

N-(4-chloro-3-nitrophenyl)-2-((4-chlorophenyl)thio)acetamide (CAS 197512-96-2), molecular formula C14H10Cl2N2O3S and molecular weight 357.21 g/mol, is a CATO reference standard with documented purity and traceability.

N-(4-chloro-3-nitrophenyl)-2-((4-chlorophenyl)thio)acetamide (C14H10Cl2N2O3S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine 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).

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 FormulaC14H10Cl2N2O3S
Molecular Weight357.21 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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2013
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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