| CAS No. | 196965-14-7 |
| Molecular Formula | C16H14F3N3OS |
| Molecular Weight | 353.36 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Compared with other compounds in its class, the molecular weight of 353.36 g/mol gives 5-(Methylthio)-N-(pyridin-3-yl)-6-(trifluoromethyl)indoline-1-carboxamide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.
CATO supplies 5-(Methylthio)-N-(pyridin-3-yl)-6-(trifluoromethyl)indoline-1-carboxamide (CAS 196965-14-7), a certified reference material (molecular formula C16H14F3N3OS, MW 353.36 g/mol) for analytical method development and quality control.
5-(Methylthio)-N-(pyridin-3-yl)-6-(trifluoromethyl)indoline-1-carboxamide (C16H14F3N3OS) contains a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage, fluorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.
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 5-(Methylthio)-N-(pyridin-3-yl)-6-(trifluoromethyl)indoline-1-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 | C16H14F3N3OS |
| Molecular Weight | 353.36 g/mol |
| Purity | 97%+ |
| Storage | Store at 2-8°C, protect from light |
| Solubility (reference) | Soluble in DMSO, DMF, methanol |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light |
| Degree of Unsaturation (DBE) | 10.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 2013 |
| Halogen Content | F-containing |
| Nitrogen Atoms | 3 |
| Sulfur Atoms | 1 |