(S,S)-()-2,6-Bis[2-(hydroxydiphenylmethyl)-1-pyrrolidinyl-methyl]-4-methylphenol
95%
- Product Code: 65698
CAS:
320714-00-9
Molecular Weight: | 638.84 g./mol | Molecular Formula: | C₄₃H₄₆N₂O₃ |
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EC Number: | MDL Number: | MFCD08276890 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2~8℃ |
Product Description:
This compound is primarily utilized in asymmetric synthesis and catalysis due to its chiral structure, which makes it effective in enantioselective reactions. It is often employed as a chiral ligand in transition metal-catalyzed processes, such as hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. Its ability to induce high enantiomeric excess in products makes it valuable in the production of pharmaceuticals, fine chemicals, and agrochemicals. Additionally, it is used in research to study chiral induction mechanisms and to develop new catalytic systems for organic synthesis. Its stability and selectivity contribute to its effectiveness in complex synthetic pathways.
Product Specification:
Test | Specification |
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Purity | 95 100% |
SPECIFIC ROTATION A20DC1CHCl3 | 45-55 |
APPEARANCE | LIGET YELLOW SOLID |
INFRARED SPECTRUM | Conforms to Structure |
PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿3,880.00 |
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1.000 | 10-20 days | ฿11,800.00 |
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(S,S)-()-2,6-Bis[2-(hydroxydiphenylmethyl)-1-pyrrolidinyl-methyl]-4-methylphenol
This compound is primarily utilized in asymmetric synthesis and catalysis due to its chiral structure, which makes it effective in enantioselective reactions. It is often employed as a chiral ligand in transition metal-catalyzed processes, such as hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. Its ability to induce high enantiomeric excess in products makes it valuable in the production of pharmaceuticals, fine chemicals, and agrochemicals. Additionally, it is used in research to study chiral induction mechanisms and to develop new catalytic systems for organic synthesis. Its stability and selectivity contribute to its effectiveness in complex synthetic pathways.
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