(11bS)-N-Benzhydryl-N-isopropyldinaphtho[2, 1-d: 1', 2'-f][1, 3, 2]dioxaphosphepin-4-amine

95%

Reagent Code: #236501
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CAS Number 1637749-69-9

science Other reagents with same CAS 1637749-69-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 539.60 g/mol
Formula C₃₆H₃₀NO₂P
badge Registry Numbers
MDL Number MFCD31707590
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used in asymmetric catalysis as a chiral ligand for transition metal-catalyzed reactions, particularly in enantioselective transformations such as hydrogenation and C–C bond formation. Its rigid dinaphthyl backbone and stereogenic center enhance stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly employed in palladium- and rhodium-catalyzed processes where high enantioselectivity is required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,610.00
inventory 250mg
10-20 days ฿2,980.00
inventory 1g
10-20 days ฿10,010.00
inventory 5g
10-20 days ฿43,430.00

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(11bS)-N-Benzhydryl-N-isopropyldinaphtho[2, 1-d: 1', 2'-f][1, 3, 2]dioxaphosphepin-4-amine
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Used in asymmetric catalysis as a chiral ligand for transition metal-catalyzed reactions, particularly in enantioselective transformations such as hydrogenation and C–C bond formation. Its rigid dinaphthyl backbone and stereogenic center enhance stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly employed in palladium- and rhodium-catalyzed processes where high enantioselectivity is required.

Used in asymmetric catalysis as a chiral ligand for transition metal-catalyzed reactions, particularly in enantioselective transformations such as hydrogenation and C–C bond formation. Its rigid dinaphthyl backbone and stereogenic center enhance stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly employed in palladium- and rhodium-catalyzed processes where high enantioselectivity is required.

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