[S(R)]-N-[(1S)-1-[3'',5''-Bis(1,1-dimethylethyl)[1,1''-biphenyl]-2-yl]-2-(diphenylphosphino)ethyl]-2-methyl-2-propanesulfinamide
95%
- Product Code: 65029
CAS:
1936438-24-2
| Molecular Weight: | 597.84 g./mol | Molecular Formula: | C₃₈H₄₈NOPS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD32697176 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, inert gas |
Product Description:
This chemical is primarily utilized in asymmetric synthesis, particularly in catalytic processes where high enantioselectivity is required. It serves as a chiral ligand in transition metal-catalyzed reactions, such as hydrogenation, cross-coupling, and allylic substitution. Its unique structure, featuring a biphenyl backbone and a sulfinamide group, enhances steric and electronic control, enabling the formation of chiral centers with high precision. This makes it valuable in the pharmaceutical industry for the synthesis of enantiomerically pure drugs and intermediates. Additionally, it finds applications in academic research for developing new methodologies in organic synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿1,701.00 |
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| 0.025 | 10-20 days | ฿7,641.00 |
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| 0.100 | 10-20 days | ฿21,591.00 |
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[S(R)]-N-[(1S)-1-[3'',5''-Bis(1,1-dimethylethyl)[1,1''-biphenyl]-2-yl]-2-(diphenylphosphino)ethyl]-2-methyl-2-propanesulfinamide
This chemical is primarily utilized in asymmetric synthesis, particularly in catalytic processes where high enantioselectivity is required. It serves as a chiral ligand in transition metal-catalyzed reactions, such as hydrogenation, cross-coupling, and allylic substitution. Its unique structure, featuring a biphenyl backbone and a sulfinamide group, enhances steric and electronic control, enabling the formation of chiral centers with high precision. This makes it valuable in the pharmaceutical industry for the synthesis of enantiomerically pure drugs and intermediates. Additionally, it finds applications in academic research for developing new methodologies in organic synthesis.
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