(S)-3-(tert-Butyl)-4-(2,6-diisopropoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole
97%
- Product Code: 38408
CAS:
2448341-44-2
| Molecular Weight: | 386.4642 g./mol | Molecular Formula: | C₂₃H₃₁O₃P |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a phosphole ring and sterically hindered substituents, makes it effective in inducing enantioselectivity in various transformations, such as hydrogenation, carbon-carbon bond formation, and other catalytic processes. It is especially valuable in the pharmaceutical industry for the production of enantiomerically pure compounds, which are crucial for developing drugs with specific biological activities and reduced side effects. Additionally, its application extends to materials science, where it can be used to design chiral polymers or advanced catalytic systems for specialized industrial processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,000.00 |
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(S)-3-(tert-Butyl)-4-(2,6-diisopropoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole
This compound is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a phosphole ring and sterically hindered substituents, makes it effective in inducing enantioselectivity in various transformations, such as hydrogenation, carbon-carbon bond formation, and other catalytic processes. It is especially valuable in the pharmaceutical industry for the production of enantiomerically pure compounds, which are crucial for developing drugs with specific biological activities and reduced side effects. Additionally, its application extends to materials science, where it can be used to design chiral polymers or advanced catalytic systems for specialized industrial processes.
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