(S)-DTBM-SEGPHOS
98%
- Product Code: 68687
CAS:
210169-40-7
| Molecular Weight: | 1179.54 g./mol | Molecular Formula: | C₇₄H₁₀₀O₈P₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09753003 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
(S)-DTBM-SEGPHOS is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in enantioselective hydrogenation, where it helps produce chiral molecules with high optical purity. This ligand is also employed in asymmetric carbon-carbon bond-forming reactions, such as cross-coupling and allylic substitution, enabling the synthesis of complex chiral intermediates for pharmaceuticals and agrochemicals. Its robust steric and electronic properties make it a preferred choice for achieving high enantioselectivity in various synthetic transformations. Additionally, (S)-DTBM-SEGPHOS is utilized in the production of fine chemicals and active pharmaceutical ingredients (APIs), where precise control over stereochemistry is critical. Its application extends to academic research and industrial processes, contributing to advancements in asymmetric synthesis.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 126 128? |
| OPTICAL PURITYEE | 97.5-100 |
| Purity | 98 100% |
| APPEARANCE | White to Light yellow to Light orange powder to crystal |
| INFRARED SPECTRUM | Conforms to Structure |
| Specific rotation a20DC1CHCl3 | 52 56 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,280.00 |
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| 0.500 | 10-20 days | ฿7,920.00 |
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| 1.000 | 10-20 days | ฿13,490.00 |
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(S)-DTBM-SEGPHOS
(S)-DTBM-SEGPHOS is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in enantioselective hydrogenation, where it helps produce chiral molecules with high optical purity. This ligand is also employed in asymmetric carbon-carbon bond-forming reactions, such as cross-coupling and allylic substitution, enabling the synthesis of complex chiral intermediates for pharmaceuticals and agrochemicals. Its robust steric and electronic properties make it a preferred choice for achieving high enantioselectivity in various synthetic transformations. Additionally, (S)-DTBM-SEGPHOS is utilized in the production of fine chemicals and active pharmaceutical ingredients (APIs), where precise control over stereochemistry is critical. Its application extends to academic research and industrial processes, contributing to advancements in asymmetric synthesis.
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