tert-Butyl 2-iodo-6-((trimethylsilyl)ethynyl)-pyridin-3-yl carbonate CAS 1142192-40-2
| CAS No. | 1142192-40-2 |
| Molecular Formula | C15H20INO3Si |
| Molecular Weight | 417.31 g/mol |
| Category | Pharmaceutical Standards / API Standards |
| Availability | In Stock |
Chemical Structure
Description
As a certified reference material (CRM), tert-Butyl 2-iodo-6-((trimethylsilyl)ethynyl)-pyridin-3-yl carbonate 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.
tert-Butyl 2-iodo-6-((trimethylsilyl)ethynyl)-pyridin-3-yl carbonate (CAS 1142192-40-2), molecular formula C15H20INO3Si and molecular weight 417.31 g/mol, is a CATO reference standard with documented purity and traceability.
The molecular framework of tert-Butyl 2-iodo-6-((trimethylsilyl)ethynyl)-pyridin-3-yl carbonate (C15H20INO3Si) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. 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.
Physical & Chemical Properties
| Molecular Formula | C15H20INO3Si |
| Molecular Weight | 417.31 g/mol |
| Appearance | Off-white to pale yellow crystalline powder. (slight halide-like odor) |
| Purity | 97%+ |
| Storage | Store at room temperature, 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; Contains ester bond; hydrolyzes under strong alkaline conditions |
| Degree of Unsaturation (DBE) | 6.0 |
| UV Absorption | UV-absorbing |
| Structural Features | Aromatic ring present |
| CAS Registry Year (est.) | 1989 |
| Halogen Content | I-containing |
| Nitrogen Atoms | 1 |
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