(3AS,8aR)-2-(2-diphenylphosphinophenyl)-3a,8a-dihydroindane[1,2-d]oxazole
98%,99%ee
- Product Code: 36729
CAS:
201409-47-4
| Molecular Weight: | 419.4542 g./mol | Molecular Formula: | C₂₈H₂₂NOP |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD32856655 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized as a ligand in transition metal catalysis, particularly in asymmetric synthesis. Its unique structure, featuring a diphenylphosphine group and an oxazole ring, makes it effective in forming stable complexes with metals like palladium, rhodium, and iridium. These complexes are employed in enantioselective reactions, such as hydrogenation, cross-coupling, and cyclization processes, which are crucial in the production of pharmaceuticals and fine chemicals. The ligand’s chiral environment enhances the selectivity of these reactions, enabling the synthesis of optically active compounds with high precision. Additionally, it finds use in academic research for developing new catalytic methodologies and exploring reaction mechanisms.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | €45.35 |
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(3AS,8aR)-2-(2-diphenylphosphinophenyl)-3a,8a-dihydroindane[1,2-d]oxazole
This chemical is primarily utilized as a ligand in transition metal catalysis, particularly in asymmetric synthesis. Its unique structure, featuring a diphenylphosphine group and an oxazole ring, makes it effective in forming stable complexes with metals like palladium, rhodium, and iridium. These complexes are employed in enantioselective reactions, such as hydrogenation, cross-coupling, and cyclization processes, which are crucial in the production of pharmaceuticals and fine chemicals. The ligand’s chiral environment enhances the selectivity of these reactions, enabling the synthesis of optically active compounds with high precision. Additionally, it finds use in academic research for developing new catalytic methodologies and exploring reaction mechanisms.
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