(11bS)-2,6-Bis(3,5-dimethylphenyl)-4-hydroxy-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide

98%

Reagent Code: #233474
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CAS Number 2757287-28-6

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 564.65 g/mol
Formula C₃₆H₃₇O₄P
thermostat Physical Properties
Boiling Point 744.9±70.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.29±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation reactions. Its rigid, sterically hindered structure enables high stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly employed with transition metal complexes such as ruthenium or rhodium catalysts to achieve high enantioselectivity in the production of chiral alcohols and amines.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,590.00
inventory 250mg
10-20 days ฿19,710.00
(11bS)-2,6-Bis(3,5-dimethylphenyl)-4-hydroxy-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 enantioselective hydrogenation reactions. Its rigid, sterically hindered structure enables high stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly employed with transition metal complexes such as ruthenium or rhodium catalysts to achieve high enantioselectivity in the production of chiral alcohols and amines.

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation reactions. Its rigid, sterically hindered structure enables high stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly employed with transition metal complexes such as ruthenium or rhodium catalysts to achieve high enantioselectivity in the production of chiral alcohols and amines.

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