Phenyl 4-bromo-2-((4-chlorophenyl)thio)thiazole-5-carboxylate CAS 1000574-07-1
| CAS No. | 1000574-07-1 |
| Molecular Formula | C16H9BrClNO2S2 |
| Molecular Weight | 426.74 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Chemical Structure
Description
As a certified reference material (CRM), Phenyl 4-bromo-2-((4-chlorophenyl)thio)thiazole-5-carboxylate meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.
CATO supplies Phenyl 4-bromo-2-((4-chlorophenyl)thio)thiazole-5-carboxylate (CAS 1000574-07-1), a certified reference material (molecular formula C16H9BrClNO2S2, MW 426.74 g/mol) for analytical method development and quality control.
Phenyl 4-bromo-2-((4-chlorophenyl)thio)thiazole-5-carboxylate (C16H9BrClNO2S2) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine/bromine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, 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 | C16H9BrClNO2S2 |
| Molecular Weight | 426.74 g/mol |
| Purity | 97%+ |
| Storage | Store at room temperature, protect from light |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate, DMSO |
| Stability | May oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; 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.) | 1988 |
| Halogen Content | Cl/Br-containing |
| Nitrogen Atoms | 1 |
| Sulfur Atoms | 2 |
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