| CAS No. | 1115871-65-2 |
| Molecular Formula | C20H19ClN2O4S2 |
| Molecular Weight | 450.96 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Compared with other compounds in its class, the molecular weight of 450.96 g/mol gives N-(4-Chlorobenzyl)-3-((4-methoxy-N-methylphenyl)sulfonamido)thiophene-2-carboxamide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
N-(4-Chlorobenzyl)-3-((4-methoxy-N-methylphenyl)sulfonamido)thiophene-2-carboxamide (CAS 1115871-65-2) is a high-purity analytical reference standard with the molecular formula C20H19ClN2O4S2 and a molecular weight of 450.96 g/mol.
N-(4-Chlorobenzyl)-3-((4-methoxy-N-methylphenyl)sulfonamido)thiophene-2-carboxamide (C20H19ClN2O4S2) contains a flavonoid core, 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).
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-(4-Chlorobenzyl)-3-((4-methoxy-N-methylphenyl)sulfonamido)thiophene-2-carboxamide 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.
| Molecular Formula | C20H19ClN2O4S2 |
| Molecular Weight | 450.96 g/mol |
| Purity | 97%+ |
| Storage | Store in a cool place (≤25°C), protect from light, keep sealed and dry |
| Solubility (reference) | Soluble in DMSO, DMF, methanol |
| Stability | May 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) | 12.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1989 |
| Halogen Content | Cl-containing |
| Nitrogen Atoms | 2 |
| Sulfur Atoms | 2 |