[S(R)]-N-[(1R)-1-[2-(Di-tert-butylphosphanyl)phenyl]phenylmethyl]-2-methyl-2-propanesulfinamide

≥95%

Reagent Code: #236111
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CAS Number 2565792-40-5

science Other reagents with same CAS 2565792-40-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 431.62 g/mol
Formula C₂₅H₃₈NOPS
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 reactions. Its steric bulk and well-defined chiral environment enable high enantioselectivity in the synthesis of complex organic molecules, making it valuable in pharmaceutical and fine chemical industries for producing single-enantiomer compounds. The tert-butyl and sulfinamide groups enhance stability and chirality transfer, while the phosphine moiety coordinates effectively with metals like palladium, rhodium, and ruthenium.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿630.00
inventory 25mg
10-20 days ฿2,400.00
inventory 100mg
10-20 days ฿7,540.00

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[S(R)]-N-[(1R)-1-[2-(Di-tert-butylphosphanyl)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 reactions. Its steric bulk and well-defined chiral environment enable high enantioselectivity in the synthesis of complex organic molecules, making it valuable in pharmaceutical and fine chemical industries for producing single-enantiomer compounds. The tert-butyl and sulfinamide groups enhance stability and chirality transfer, while the phosphine moiet

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling reactions. Its steric bulk and well-defined chiral environment enable high enantioselectivity in the synthesis of complex organic molecules, making it valuable in pharmaceutical and fine chemical industries for producing single-enantiomer compounds. The tert-butyl and sulfinamide groups enhance stability and chirality transfer, while the phosphine moiety coordinates effectively with metals like palladium, rhodium, and ruthenium.

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