(R)-5-(8,9,10,11,12,13,14,15-Octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-5H-dibenzo[b,f]azepine

95%

Reagent Code: #229471
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CAS Number 2070926-11-1

science Other reagents with same CAS 2070926-11-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 515.59 g/mol
Formula C₃₄H₃₀NO₂P
thermostat Physical Properties
Boiling Point 688.0±65.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation and cross-coupling. Its rigid, sterically defined structure enables high enantioselectivity in the synthesis of pharmaceutical intermediates and fine chemicals. Commonly employed in the production of optically active compounds where precise stereochemical control is critical. Also applied in research settings for developing new catalytic processes and improving reaction efficiency in enantioselective transformations.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿6,900.00
250mg
10-20 days ฿11,730.00
1g
10-20 days ฿31,660.00
(R)-5-(8,9,10,11,12,13,14,15-Octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-5H-dibenzo[b,f]azepine
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Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation and cross-coupling. Its rigid, sterically defined structure enables high enantioselectivity in the synthesis of pharmaceutical intermediates and fine chemicals. Commonly employed in the production of optically active compounds where precise stereochemical control is critical. Also applied in research settings for developing new catalytic processes and improving reaction efficiency i

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation and cross-coupling. Its rigid, sterically defined structure enables high enantioselectivity in the synthesis of pharmaceutical intermediates and fine chemicals. Commonly employed in the production of optically active compounds where precise stereochemical control is critical. Also applied in research settings for developing new catalytic processes and improving reaction efficiency in enantioselective transformations.

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