(4R,4'R,5S,5'S)-2,2'-(1-Methylethylidene)bis[4,5-dihydro-4,5-diphenyloxazole]

≥98%,99%e.e.

  • Product Code: 59711
  CAS:    157904-67-1
Molecular Weight: 486.6 g./mol Molecular Formula: C₃₃H₃₀N₂O₂
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: room temperature, dry
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 enantiomerically pure compounds, which are essential in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). Its robust structure and ability to induce high enantioselectivity make it valuable in the development of drugs, agrochemicals, and fine chemicals. Additionally, it is used in academic and industrial research to explore new catalytic methodologies and optimize existing synthetic routes.
Product Specification:
Test Specification
APPEARANCE White to Yellow to Beige to Brown Powder or Crystals or solids
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $296.99
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-
0.250 10-20 days $639.88
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(4R,4'R,5S,5'S)-2,2'-(1-Methylethylidene)bis[4,5-dihydro-4,5-diphenyloxazole]
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 enantiomerically pure compounds, which are essential in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). Its robust structure and ability to induce high enantioselectivity make it valuable in the development of drugs, agrochemicals, and fine chemicals. Additionally, it is used in academic and industrial research to explore new catalytic methodologies and optimize existing synthetic routes.
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