(11bS)-4-Hydroxy-2,6-bis(4-nitrophenyl)-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide

97%

Reagent Code: #236815
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CAS Number 2129645-31-2

science Other reagents with same CAS 2129645-31-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 598.539 g/mol
Formula C₃₂H₂₇N₂O₈P
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and C–C bond formation. Its rigid, bidentate structure enables high enantioselectivity in the synthesis of chiral molecules, making it valuable in pharmaceutical and fine chemical industries for producing single-enantiomer compounds. The presence of nitrophenyl groups enhances electronic properties that improve catalytic activity and stability of metal complexes. Commonly employed in research settings for developing enantioselective synthetic routes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,150.00
(11bS)-4-Hydroxy-2,6-bis(4-nitrophenyl)-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide
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Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and C–C bond formation. Its rigid, bidentate structure enables high enantioselectivity in the synthesis of chiral molecules, making it valuable in pharmaceutical and fine chemical industries for producing single-enantiomer compounds. The presence of nitrophenyl groups enhances electronic properties that improve catalytic activity and stability of metal complexes. Commonly

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and C–C bond formation. Its rigid, bidentate structure enables high enantioselectivity in the synthesis of chiral molecules, making it valuable in pharmaceutical and fine chemical industries for producing single-enantiomer compounds. The presence of nitrophenyl groups enhances electronic properties that improve catalytic activity and stability of metal complexes. Commonly employed in research settings for developing enantioselective synthetic routes.

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