| CAS No. | 2159-40-2 |
| Molecular Formula | C14H9BrO3 |
| Molecular Weight | 305.12 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
CATO supplies 2-(2-chlorobenzyl)-4-methyl-2h-thieno[3,4-e][1,2,4]thiadiazin-3(4h)-one 1,1-dioxide 2159-40-2 AR-1C6609 (CAS 2159-40-2), a certified reference material (molecular formula C14H9BrO3, MW 305.12 g/mol) for analytical method development and quality control.
Owing to a carboxylic acid group, a hydroxyl group, an ether linkage, bromine substitution, a polycyclic aromatic system, 2-(2-chlorobenzyl)-4-methyl-2h-thieno[3,4-e][1,2,4]thiadiazin-3(4h)-one 1,1-dioxide 2159-40-2 AR-1C6609 is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 305.12 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).
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 2-(2-chlorobenzyl)-4-methyl-2h-thieno[3,4-e][1,2,4]thiadiazin-3(4h)-one 1,1-dioxide 2159-40-2 AR-1C6609 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 | C14H9BrO3 |
| Molecular Weight | 305.12 g/mol |
| Appearance | Pale yellow to yellow crystalline powder. (slight halide-like odor) |
| Purity | 97%+ |
| Storage | Store at 2-8°C, protect from light, keep sealed and dry |
| Solubility (reference) | Soluble in chloroform, dichloromethane, ethyl acetate, DMSO |
| 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) | 10.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1957 |
| Halogen Content | Br-containing |