(R)-N-((S)-(2-(Diphenylphosphanyl)-4,5-dimethoxyphenyl)(naphthalen-1-yl)methyl)-2-methylpropane-2-sulfinamide

95%

Reagent Code: #231340
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CAS Number 2417456-74-5

science Other reagents with same CAS 2417456-74-5

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inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

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 phosphine and sulfinamide functional groups coordinate effectively with metals like palladium, rhodium, and ruthenium, enabling high enantioselectivity in the synthesis of chiral molecules. Commonly employed in pharmaceutical and fine chemical industries for the production of enantiomerically pure compounds. The steric bulk and electronic properties of the ligand framework enhance catalytic efficiency and stereochemical control.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿7,350.00
inventory 50mg
10-20 days ฿14,690.00
inventory 100mg
10-20 days ฿27,520.00

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(R)-N-((S)-(2-(Diphenylphosphanyl)-4,5-dimethoxyphenyl)(naphthalen-1-yl)methyl)-2-methylpropane-2-sulfinamide
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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 phosphine and sulfinamide functional groups coordinate effectively with metals like palladium, rhodium, and ruthenium, enabling high enantioselectivity in the synthesis of chiral molecules. Commonly employed in pharmaceutical and fine chemical industries for the production of enantiomerically pure compounds. The steric bulk and electronic

Used as a chiral ligand in asymmetric catalysis, particularly in transition-metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling reactions. Its phosphine and sulfinamide functional groups coordinate effectively with metals like palladium, rhodium, and ruthenium, enabling high enantioselectivity in the synthesis of chiral molecules. Commonly employed in pharmaceutical and fine chemical industries for the production of enantiomerically pure compounds. The steric bulk and electronic properties of the ligand framework enhance catalytic efficiency and stereochemical control.

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