(R)-()-2,2'-Bis(di-p-tolylphosphino)-1,1'-binaphthyl

98%

  • Product Code: 113862
  CAS:    99646-28-3
Molecular Weight: 678.78 g./mol Molecular Formula: C₄₈H₄₀P₂
EC Number: MDL Number: MFCD01311709
Melting Point: 255-257 °C Boiling Point:
Density: Storage Condition: room temperature
Product Description: This chemical 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. Its application extends to carbon-carbon bond-forming reactions, such as Suzuki-Miyaura and Heck couplings, enabling the creation of complex organic compounds with precise stereochemistry. Additionally, it is employed in the synthesis of chiral ligands and catalysts, further enhancing its utility in asymmetric synthesis. Its robust structure and excellent chiral induction make it a valuable tool in organic and medicinal chemistry research.
Product Specification:
Test Specification
Melting Point 254-259
Purity (%) 98-100
Specific Rotation 155-165
Appearance White Crystal Powder
Appearance White Crystal Powder
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days £16.28
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1.000 10-20 days £63.33
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(R)-()-2,2'-Bis(di-p-tolylphosphino)-1,1'-binaphthyl
This chemical 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. Its application extends to carbon-carbon bond-forming reactions, such as Suzuki-Miyaura and Heck couplings, enabling the creation of complex organic compounds with precise stereochemistry. Additionally, it is employed in the synthesis of chiral ligands and catalysts, further enhancing its utility in asymmetric synthesis. Its robust structure and excellent chiral induction make it a valuable tool in organic and medicinal chemistry research.
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