![(4S)-2-[2-(diphenylphosphino)phenyl]-4,5-dihydro-5,5-dimethyl-4-(1-methylethyl)-oxazole molecular structure](/images/molecules/-4s--2--2--diphenylphosphino-phenyl--4-5-dihydro-5-5-dimethyl-4--1-methylethyl--oxazole-1152313-76-2.png)
Ordering
Available Variants500 mg
CHA.88085-500mg
Price
€184.80
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
500 mg | CHA.88085-500mg | €184.80 |
97%
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) | C26H28NOP |
|---|---|
| CAS Number | 1152313-76-2 |
| Molecular Weight | 401.48 |
| NACRES | NA.22 |
| PubChem Substance ID | 329763666 |
| UNSPSC Code | 12352005 |
| MDL number | MFCD16621462 |
Safety Information Handling visibility
| pictograms |
GHS06
 GHS06
|
|---|---|
| signalword | Danger |
| hcodes | H301,H315,H319,H335,H413 |
| pcodes | P261 - P264 - P273 - P301 + P310 - P302 + P352 - P305 + P351 + P338 |
| Hazard Classifications | Acute Tox. 3 Oral - Aquatic Chronic 4 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3 |
| target_organs | Respiratory system |
| Storage Class | 6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects |
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
Technical Overview & Applications Use-case context
(4S)-2-[2-(diphenylphosphino)phenyl]-4,5-dihydro-5,5-dimethyl-4-(1-methylethyl)-oxazole, with the CAS registry number 1152313-76-2, is a complex organic compound that has garnered significant attention in the realm of organometallic chemistry. This molecule features a unique oxazole backbone, substituted with a diphenylphosphino group and an isopropyl moiety, rendering it a valuable ligand in various catalytic reactions. The compounds chiral nature, as denoted by the (4S) designation, is crucial for its applications in asymmetric synthesis, where it can facilitate the formation of enantiomerically enriched products. As such, researchers have explored its potential in numerous catalytic transformations, including cross-coupling reactions and hydrogenations, highlighting its versatility and efficacy as a chiral ligand. Further studies are warranted to fully elucidate its properties and potential applications.
