(S)-2-[(Diphenylphosphino)methyl]pyrrolidine
98%
- Product Code: 70436
CAS:
60261-46-3
Molecular Weight: | 269.321161 g./mol | Molecular Formula: | C₁₇H₂₀NP |
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EC Number: | MDL Number: | MFCD16621443 | |
Melting Point: | Boiling Point: | 387.1±15.0 °C | |
Density: | 1.043 g/mL at 25 °C | Storage Condition: | 2-8°C, away from light |
Product Description:
(S)-2-[(Diphenylphosphino)methyl]pyrrolidine is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective hydrogenation, where it helps produce chiral molecules with high optical purity, essential in the synthesis of pharmaceuticals and fine chemicals. This ligand is also employed in asymmetric allylic alkylation and cross-coupling reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds with high stereocontrol. Its application extends to the development of chiral catalysts for organic transformations, contributing to the efficient and selective synthesis of complex molecules in medicinal chemistry and materials science.
Product Specification:
Test | Specification |
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APPEARANCE | Colorless to light yellow Liquid |
PURITY | 97.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.050 | 10-20 days | ฿4,820.00 |
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0.250 | 10-20 days | ฿13,890.00 |
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(S)-2-[(Diphenylphosphino)methyl]pyrrolidine
(S)-2-[(Diphenylphosphino)methyl]pyrrolidine is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective hydrogenation, where it helps produce chiral molecules with high optical purity, essential in the synthesis of pharmaceuticals and fine chemicals. This ligand is also employed in asymmetric allylic alkylation and cross-coupling reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds with high stereocontrol. Its application extends to the development of chiral catalysts for organic transformations, contributing to the efficient and selective synthesis of complex molecules in medicinal chemistry and materials science.
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