(S)-2-(7'-(Bis(3,5-di-tert-butylphenyl)phosphino)-2,2',3,3'-tetrahydro-1,1'-spirobi[inden]-7-yl)-4,5-dihydrooxazole

98%

  • Product Code: 70604
  CAS:    1040274-18-7
Molecular Weight: 697.97 g./mol Molecular Formula: C₄₈H₆₀NOP
EC Number: MDL Number: MFCD21362521
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C
Product Description: This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a spirobi[inden] backbone and a phosphine group, makes it highly effective in inducing enantioselectivity in various organic transformations. It is commonly employed in hydrogenation reactions, where it helps produce chiral molecules with high enantiomeric purity, which are crucial in the synthesis of pharmaceuticals and fine chemicals. Additionally, its sterically hindered tert-butyl groups enhance stability and selectivity, making it suitable for challenging catalytic processes. This ligand is also explored in C-C bond-forming reactions, such as cross-coupling and cycloaddition, contributing to the development of complex organic compounds with precise stereochemistry.
Product Specification:
Test Specification
APPEARANCE White to off-white Solid
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.010 10-20 days ฿9,080.00
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(S)-2-(7'-(Bis(3,5-di-tert-butylphenyl)phosphino)-2,2',3,3'-tetrahydro-1,1'-spirobi[inden]-7-yl)-4,5-dihydrooxazole
This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a spirobi[inden] backbone and a phosphine group, makes it highly effective in inducing enantioselectivity in various organic transformations. It is commonly employed in hydrogenation reactions, where it helps produce chiral molecules with high enantiomeric purity, which are crucial in the synthesis of pharmaceuticals and fine chemicals. Additionally, its sterically hindered tert-butyl groups enhance stability and selectivity, making it suitable for challenging catalytic processes. This ligand is also explored in C-C bond-forming reactions, such as cross-coupling and cycloaddition, contributing to the development of complex organic compounds with precise stereochemistry.
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