(R)-3-(Tert-butyl)-4-(2,6-dimethoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole
97%
- Product Code: 68651
CAS:
1338454-03-7
| Molecular Weight: | 330.35 g./mol | Molecular Formula: | C₁₉H₂₃O₃P |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31630704 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand or catalyst. Its unique structure, featuring a phosphole ring and tert-butyl group, makes it highly effective in facilitating enantioselective reactions, particularly in the synthesis of complex organic molecules. It is often employed in pharmaceutical research to produce chiral intermediates for drug development, ensuring high enantiomeric purity. Additionally, its application extends to material science, where it aids in the creation of chiral polymers and advanced materials with specific optical properties. The compound’s stability and selectivity make it a valuable tool in organic chemistry laboratories for designing and optimizing catalytic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,933.00 |
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| 0.250 | 10-20 days | ฿8,163.00 |
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| 1.000 | 10-20 days | ฿24,453.00 |
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(R)-3-(Tert-butyl)-4-(2,6-dimethoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole
This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand or catalyst. Its unique structure, featuring a phosphole ring and tert-butyl group, makes it highly effective in facilitating enantioselective reactions, particularly in the synthesis of complex organic molecules. It is often employed in pharmaceutical research to produce chiral intermediates for drug development, ensuring high enantiomeric purity. Additionally, its application extends to material science, where it aids in the creation of chiral polymers and advanced materials with specific optical properties. The compound’s stability and selectivity make it a valuable tool in organic chemistry laboratories for designing and optimizing catalytic processes.
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