(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
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
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
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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