(4R,4'R)-2,2'-(Cyclopentane-1,1-diyl)bis(4-benzyl-4,5-dihydrooxazole)

98%

  • Product Code: 59697
  CAS:    2005443-99-0
Molecular Weight: 388.50 g./mol Molecular Formula: C₂₅H₂₈N₂O₂
EC Number: MDL Number: MFCD32201202
Melting Point: Boiling Point: 524.0±33.0 °C
Density: 1.21±0.1 g/cm3 Storage Condition: 2-8°C
Product Description: This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce optically active compounds with high enantiomeric excess. Its rigid structure and specific stereochemistry make it effective in controlling the spatial arrangement of reactants, leading to the formation of desired chiral products. This compound is especially valuable in the pharmaceutical industry for synthesizing enantiomerically pure drugs and intermediates, ensuring higher efficacy and reduced side effects. Additionally, it finds application in academic research for developing new asymmetric methodologies and studying chiral induction mechanisms.
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
0.050 10-20 days ฿1,990.00
+
-
0.250 10-20 days ฿8,730.00
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-
(4R,4'R)-2,2'-(Cyclopentane-1,1-diyl)bis(4-benzyl-4,5-dihydrooxazole)
This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce optically active compounds with high enantiomeric excess. Its rigid structure and specific stereochemistry make it effective in controlling the spatial arrangement of reactants, leading to the formation of desired chiral products. This compound is especially valuable in the pharmaceutical industry for synthesizing enantiomerically pure drugs and intermediates, ensuring higher efficacy and reduced side effects. Additionally, it finds application in academic research for developing new asymmetric methodologies and studying chiral induction mechanisms.
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