N-((3-chloro-5-(trifluoromethyl)pyridin-2-yl)carbamoyl)-4-methylbenzenesulfonamide CAS 144848-79-3

Purity 97%+In StockPharmaceutical Standards
CAS No.144848-79-3
Molecular FormulaC14H11ClF3N3O3S
Molecular Weight393.77 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-((3-chloro-5-(trifluoromethyl)pyridin-2-yl)carbamoyl)-4-methylbenzenesulfonamide CAS 144848-79-3 chemical structure

Description

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution, N-((3-chloro-5-(trifluoromethyl)pyridin-2-yl)carbamoyl)-4-methylbenzenesulfonamide is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 393.77 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

N-((3-chloro-5-(trifluoromethyl)pyridin-2-yl)carbamoyl)-4-methylbenzenesulfonamide (CAS 144848-79-3) is a high-purity analytical reference standard with the molecular formula C14H11ClF3N3O3S and a molecular weight of 393.77 g/mol.

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 N-((3-chloro-5-(trifluoromethyl)pyridin-2-yl)carbamoyl)-4-methylbenzenesulfonamide 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 FormulaC14H11ClF3N3O3S
Molecular Weight393.77 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1998
Halogen ContentF/Cl-containing
Nitrogen Atoms3
Sulfur Atoms1

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