N-((11bR)-2,6-Dimethyl-4-oxidodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-1,1,1-trifluoromethanesulfonamide

98%

Reagent Code: #215958
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CAS Number 2757287-61-7

science Other reagents with same CAS 2757287-61-7

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Weight 507.42 g/mol
Formula C₂₃H₁₇F₃NO₅PS
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a chiral ligand precursor in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as enantioselective hydrogenation and cross-coupling. Its rigid dinaphthyl backbone and phosphorus center with defined stereochemistry make it effective for inducing high enantioselectivity in the synthesis of pharmaceuticals and fine chemicals. Commonly employed in the development of chiral phosphine ligands after modification, it plays a key role in producing single-enantiomer compounds important in drug manufacturing.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿9,800.00
inventory 100mg
10-20 days ฿14,680.00
inventory 250mg
10-20 days ฿23,480.00

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N-((11bR)-2,6-Dimethyl-4-oxidodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-1,1,1-trifluoromethanesulfonamide
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Used as a chiral ligand precursor in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as enantioselective hydrogenation and cross-coupling. Its rigid dinaphthyl backbone and phosphorus center with defined stereochemistry make it effective for inducing high enantioselectivity in the synthesis of pharmaceuticals and fine chemicals. Commonly employed in the development of chiral phosphine ligands after modification, it plays a key role in producing single-enantiomer compounds

Used as a chiral ligand precursor in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as enantioselective hydrogenation and cross-coupling. Its rigid dinaphthyl backbone and phosphorus center with defined stereochemistry make it effective for inducing high enantioselectivity in the synthesis of pharmaceuticals and fine chemicals. Commonly employed in the development of chiral phosphine ligands after modification, it plays a key role in producing single-enantiomer compounds important in drug manufacturing.

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