2-(4-Bromo-3-Hydroxy-2-Quinolinyl)-N-[3-[[4-(Dibutylamino)-6-Fluoro-1,3,5-Triazin-2-Yl]Oxy]Phenyl]-2,3-Dihydro-1,3-Dioxo-1H-Indene-5-Carboxamide CAS 94232-75-4
| CAS No. | 94232-75-4 |
| Molecular Formula | C36H32BrFN6O5 |
| Molecular Weight | 727.58 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Chemical Structure
Description
The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.
2-(4-Bromo-3-Hydroxy-2-Quinolinyl)-N-[3-[[4-(Dibutylamino)-6-Fluoro-1,3,5-Triazin-2-Yl]Oxy]Phenyl]-2,3-Dihydro-1,3-Dioxo-1H-Indene-5-Carboxamide (CAS 94232-75-4) is a high-purity analytical reference standard with the molecular formula C36H32BrFN6O5 and a molecular weight of 727.58 g/mol.
2-(4-Bromo-3-Hydroxy-2-Quinolinyl)-N-[3-[[4-(Dibutylamino)-6-Fluoro-1,3,5-Triazin-2-Yl]Oxy]Phenyl]-2,3-Dihydro-1,3-Dioxo-1H-Indene-5-Carboxamide (C36H32BrFN6O5) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine/bromine 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. 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.
Physical & Chemical Properties
| Molecular Formula | C36H32BrFN6O5 |
| Molecular Weight | 727.58 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) | 23.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1983 |
| Halogen Content | F/Br-containing |
| Nitrogen Atoms | 6 |
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