(3aS,3'aS,8aR,8'aR)-2,2'-Cyclohexylidenebis[3a,8a-dihydro-dihydro-8H-indeno[1,2-d]oxazole

95% 99%ee

  • Product Code: 236857
  CAS:    2341858-19-1
Molecular Weight: 412.52 g./mol Molecular Formula: C₂₇H₂₈N₂O₂
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, Inert Gas
Product Description: Used as a chiral auxiliary or asymmetric synthesis reagent in organic chemistry, particularly in enantioselective transformations. Its rigid, sterically defined structure makes it valuable in catalysis, where it helps control stereochemistry in carbon-carbon bond-forming reactions. Commonly employed in asymmetric aldol reactions, alkylations, and Diels-Alder cyclizations to achieve high enantiomeric excess. Also utilized in the development of pharmaceutical intermediates where precise stereochemical control is critical. Its bidentate oxazoline framework allows coordination to metal centers, enabling use in chiral ligand-metal catalyzed processes.
Sizes / Availability / Pricing:
Size Availability Price Quantity
0.100 10-20 days Ft43,083.91
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0.250 10-20 days Ft69,564.75
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1.000 10-20 days Ft263,757.60
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(3aS,3'aS,8aR,8'aR)-2,2'-Cyclohexylidenebis[3a,8a-dihydro-dihydro-8H-indeno[1,2-d]oxazole
Used as a chiral auxiliary or asymmetric synthesis reagent in organic chemistry, particularly in enantioselective transformations. Its rigid, sterically defined structure makes it valuable in catalysis, where it helps control stereochemistry in carbon-carbon bond-forming reactions. Commonly employed in asymmetric aldol reactions, alkylations, and Diels-Alder cyclizations to achieve high enantiomeric excess. Also utilized in the development of pharmaceutical intermediates where precise stereochemical control is critical. Its bidentate oxazoline framework allows coordination to metal centers, enabling use in chiral ligand-metal catalyzed processes.
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