[S(R)]-N-[(R)-[2-(Dicyclohexylphosphanyl)phenyl](4-methoxyphenyl)methyl]-N,2-dimethyl-2-propanesulfinamide

≥95%

Reagent Code: #236107
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CAS Number 2565792-29-0

science Other reagents with same CAS 2565792-29-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 511.70 g/mol
Formula C₃₁H₄₆NO₂PS
inventory_2 Storage & Handling
Storage 2-8°C, avoid light, inert gas storage

description Product Description

This compound is widely used as a chiral ligand precursor in asymmetric catalysis, particularly in transition-metal-catalyzed reactions. It plays a key role in the synthesis of enantiomerically enriched compounds, making it valuable in pharmaceutical and fine chemical industries. Due to its well-defined stereochemistry and bulky dicyclohexylphosphanyl group, it forms highly selective catalysts for asymmetric transformations such as hydrogenation, C–C bond formation, and allylic alkylation. Its sulfinamide moiety allows for easy handling and purification, while the chiral centers ensure high stereocontrol when coordinated to metals like palladium, rhodium, or ruthenium. It is especially effective in reactions requiring high enantioselectivity and catalyst turnover.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿1,480.00
inventory 25mg
10-20 days ฿4,210.00
inventory 100mg
10-20 days ฿12,550.00

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[S(R)]-N-[(R)-[2-(Dicyclohexylphosphanyl)phenyl](4-methoxyphenyl)methyl]-N,2-dimethyl-2-propanesulfinamide
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This compound is widely used as a chiral ligand precursor in asymmetric catalysis, particularly in transition-metal-catalyzed reactions. It plays a key role in the synthesis of enantiomerically enriched compounds, making it valuable in pharmaceutical and fine chemical industries. Due to its well-defined stereochemistry and bulky dicyclohexylphosphanyl group, it forms highly selective catalysts for asymmetric transformations such as hydrogenation, C–C bond formation, and allylic alkylation. Its sulfinamid

This compound is widely used as a chiral ligand precursor in asymmetric catalysis, particularly in transition-metal-catalyzed reactions. It plays a key role in the synthesis of enantiomerically enriched compounds, making it valuable in pharmaceutical and fine chemical industries. Due to its well-defined stereochemistry and bulky dicyclohexylphosphanyl group, it forms highly selective catalysts for asymmetric transformations such as hydrogenation, C–C bond formation, and allylic alkylation. Its sulfinamide moiety allows for easy handling and purification, while the chiral centers ensure high stereocontrol when coordinated to metals like palladium, rhodium, or ruthenium. It is especially effective in reactions requiring high enantioselectivity and catalyst turnover.

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