[S(R)]-N-[(S)-[3,5-Bis(1,1-dimethylethyl)-4 methoxyphenyl][2-(dicyclohexylphosphino)phenyl]methyl]-2-methyl-2-propanesulfinamide
95%
- Product Code: 68872
CAS:
2241598-31-0
| Molecular Weight: | 625.9 g./mol | Molecular Formula: | C₃₈H₆₀NO₂PS |
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| Density: | Storage Condition: | room temperature |
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 other carbon-carbon bond-forming reactions. Its structure, featuring a sulfinamide group and a bulky phosphine moiety, makes it highly effective in controlling the stereochemistry of the reaction products. This compound is especially valuable in the pharmaceutical industry for the synthesis of chiral intermediates and active pharmaceutical ingredients (APIs), where precise stereochemical control is critical. Additionally, it finds applications in academic research for developing new catalytic methodologies and exploring asymmetric transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | $391.40 |
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| 0.100 | 10-20 days | $1,131.50 |
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[S(R)]-N-[(S)-[3,5-Bis(1,1-dimethylethyl)-4 methoxyphenyl][2-(dicyclohexylphosphino)phenyl]methyl]-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 other carbon-carbon bond-forming reactions. Its structure, featuring a sulfinamide group and a bulky phosphine moiety, makes it highly effective in controlling the stereochemistry of the reaction products. This compound is especially valuable in the pharmaceutical industry for the synthesis of chiral intermediates and active pharmaceutical ingredients (APIs), where precise stereochemical control is critical. Additionally, it finds applications in academic research for developing new catalytic methodologies and exploring asymmetric transformations.
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