[S(R)]-N-[(S)-1-[5-(Diphenylphosphino)-9,9-dimethyl-9H-xanthen-4-yl]ethyl]-2-methyl-2-propanesulfinamide
95%
- Product Code: 68846
CAS:
2162939-90-2
Molecular Weight: | 541.7 g./mol | Molecular Formula: | C₃₃H₃₆NO₂PS |
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EC Number: | MDL Number: | ||
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Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in asymmetric synthesis, particularly in catalytic asymmetric reactions. It serves as a chiral ligand in transition metal catalysis, enabling the production of enantiomerically pure compounds. Its application is significant in pharmaceutical synthesis, where it aids in creating chiral intermediates for active pharmaceutical ingredients (APIs). Additionally, it is employed in the synthesis of complex organic molecules, including natural products and fine chemicals, due to its ability to induce high enantioselectivity and yield in reactions such as hydrogenation, cross-coupling, and allylic substitution. Its robust structure and stereochemical control make it a valuable tool in advanced organic chemistry research and industrial processes.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.025 | 10-20 days | ฿7,011.00 |
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0.100 | 10-20 days | ฿11,700.00 |
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0.500 | 10-20 days | ฿46,800.00 |
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[S(R)]-N-[(S)-1-[5-(Diphenylphosphino)-9,9-dimethyl-9H-xanthen-4-yl]ethyl]-2-methyl-2-propanesulfinamide
This chemical is primarily used in asymmetric synthesis, particularly in catalytic asymmetric reactions. It serves as a chiral ligand in transition metal catalysis, enabling the production of enantiomerically pure compounds. Its application is significant in pharmaceutical synthesis, where it aids in creating chiral intermediates for active pharmaceutical ingredients (APIs). Additionally, it is employed in the synthesis of complex organic molecules, including natural products and fine chemicals, due to its ability to induce high enantioselectivity and yield in reactions such as hydrogenation, cross-coupling, and allylic substitution. Its robust structure and stereochemical control make it a valuable tool in advanced organic chemistry research and industrial processes.
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