(4S)-2-[(1S)-7'-(Diphenylphosphino)-2,2',3,3'-tetrahydro-1,1'-spirobi[1H-inden]-7-yl]-4,5-dihydro-4-(phenylmethyl)oxazole

≥98%,≥99% e.e.

Reagent Code: #59712
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CAS Number 913829-88-6

science Other reagents with same CAS 913829-88-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 563.7 g/mol
Formula C₃₉H₃₄NOP
thermostat Physical Properties
Melting Point 164-166 °C
Boiling Point 702.3±60.0 °C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the field of asymmetric catalysis, particularly in the synthesis of chiral molecules. Its structure, featuring a diphenylphosphino group and a spirobiindane backbone, makes it an effective ligand for transition metal catalysts. These catalysts are employed in various enantioselective reactions, such as hydrogenation, carbon-carbon bond formation, and other transformations critical in pharmaceutical and fine chemical industries. The chiral environment created by this ligand ensures high selectivity and efficiency in producing optically active compounds, which are essential for developing drugs and other bioactive molecules. Its application is particularly valuable in the production of intermediates for active pharmaceutical ingredients (APIs) where chirality plays a crucial role in the efficacy and safety of the final product.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿6,741.00
inventory 100mg
10-20 days ฿20,160.00

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(4S)-2-[(1S)-7'-(Diphenylphosphino)-2,2',3,3'-tetrahydro-1,1'-spirobi[1H-inden]-7-yl]-4,5-dihydro-4-(phenylmethyl)oxazole
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This compound is primarily utilized in the field of asymmetric catalysis, particularly in the synthesis of chiral molecules. Its structure, featuring a diphenylphosphino group and a spirobiindane backbone, makes it an effective ligand for transition metal catalysts. These catalysts are employed in various enantioselective reactions, such as hydrogenation, carbon-carbon bond formation, and other transformations critical in pharmaceutical and fine chemical industries. The chiral environment created by this

This compound is primarily utilized in the field of asymmetric catalysis, particularly in the synthesis of chiral molecules. Its structure, featuring a diphenylphosphino group and a spirobiindane backbone, makes it an effective ligand for transition metal catalysts. These catalysts are employed in various enantioselective reactions, such as hydrogenation, carbon-carbon bond formation, and other transformations critical in pharmaceutical and fine chemical industries. The chiral environment created by this ligand ensures high selectivity and efficiency in producing optically active compounds, which are essential for developing drugs and other bioactive molecules. Its application is particularly valuable in the production of intermediates for active pharmaceutical ingredients (APIs) where chirality plays a crucial role in the efficacy and safety of the final product.

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