(S,S)-()-2,6-Bis[2-(hydroxydiphenylmethyl)-1-pyrrolidinyl-methyl]-4-methylphenol

95%

Reagent Code: #65698
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CAS Number 320714-00-9

science Other reagents with same CAS 320714-00-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 638.84 g/mol
Formula C₄₃H₄₆N₂O₃
badge Registry Numbers
MDL Number MFCD08276890
inventory_2 Storage & Handling
Storage 2~8℃

description 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.

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Test Parameter Specification
Purity 95-100%
Specific Rotation (A20/D/C1/CHCl3) 45-55
Appearance Light Yellow Solid
Infrared Spectrum Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿11,800.00
inventory 250mg
10-20 days ฿3,880.00

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(S,S)-()-2,6-Bis[2-(hydroxydiphenylmethyl)-1-pyrrolidinyl-methyl]-4-methylphenol
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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

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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