[S(R)]-N-[(R)-[2-(Diadamantanphosphino)phenyl]phenylmethyl]-2-methyl-2-propanesulfinamide

≥95%

Reagent Code: #236109
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CAS Number 2565792-31-4

science Other reagents with same CAS 2565792-31-4

blur_circular Chemical Specifications

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Weight 587.85 g/mol
Formula C₃₇H₅₀NOPS
inventory_2 Storage & Handling
Storage 2-8°C, avoid light, inert gas storage

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling. Its rigid, sterically hindered structure enhances enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. The phosphine group binds strongly to metals like palladium, rhodium, or ruthenium, while the sulfinamide moiety contributes to stereocontrol. Effective in low catalyst loadings, it enables high yield and ee in the production of chiral intermediates.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿400.00
inventory 25mg
10-20 days ฿1,850.00
inventory 100mg
10-20 days ฿7,190.00

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[S(R)]-N-[(R)-[2-(Diadamantanphosphino)phenyl]phenylmethyl]-2-methyl-2-propanesulfinamide
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Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling. Its rigid, sterically hindered structure enhances enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. The phosphine group binds strongly to metals like palladium, rhodium, or ruthenium, while the sulfinamide moiety contributes to stereocontrol. Effective in low catalyst loadings, it enables high
Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling. Its rigid, sterically hindered structure enhances enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. The phosphine group binds strongly to metals like palladium, rhodium, or ruthenium, while the sulfinamide moiety contributes to stereocontrol. Effective in low catalyst loadings, it enables high yield and ee in the production of chiral intermediates.
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