Ordering
Available Variants500 mg
CHA.17843-500mg
Price
€89.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
500 mg | CHA.17843-500mg | €89.60 |
solid
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
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Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C12H16N2O |
|---|---|
| CAS Number | 117408-98-7 |
| Molecular Weight | 204.27 |
| UNSPSC Code | 12352300 |
| PubChem Substance ID | 329766431 |
| NACRES | NA.22 |
| MDL number | MFCD22200533 |
| Form | solid |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H315,H319 |
| pcodes | P264 - P280 - P302 + P352 - P305 + P351 + P338 - P332 + P313 - P337 + P313 |
| Hazard Classifications | Eye Irrit. 2 - Skin Irrit. 2 |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
(S)-4-tert-Butyl-2-(2-pyridyl)oxazoline, with a CAS number of 117408-98-7, is a versatile chiral ligand utilized in various asymmetric catalytic reactions. This compound has been extensively employed in metal-catalyzed transformations, including cycloaddition reactions and hydrogenations, to produce enantiomerically enriched products. The presence of the 2-pyridyl substituent enables the formation of stable complexes with metal centers, while the tert-butyl group provides steric protection, enhancing the ligands ability to induce asymmetry. As a result, (S)-4-tert-Butyl-2-(2-pyridyl)oxazoline has become a valuable tool in the synthesis of complex molecules, particularly in the pharmaceutical and agrochemical industries, where the production of enantiopure compounds is crucial. Its high purity and stability make it an ideal choice for researchers and manufacturers seeking to develop efficient and selective catalytic processes.
