[S(R)]-N-[(R)-[(3-(Benzyloxy)-2-(dicyclohexylphosphino)phenyl)phenylmethyl]-2-methyl-2-propanesulfinamide

≥95%

Reagent Code: #236112
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CAS Number 2565792-41-6

science Other reagents with same CAS 2565792-41-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 589.82 g/mol
Formula C₃₆H₄₈NO₂PS
inventory_2 Storage & Handling
Storage 2-8°C, avoid light, inert gas storage

description Product Description

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations, particularly in rhodium- or ruthenium-catalyzed asymmetric hydrogenation reactions. It is especially effective in the synthesis of chiral amines, amino acids, and other nitrogen-containing compounds where high enantiomeric excess is required. Due to its rigid, sterically demanding structure and well-defined stereochemistry, it helps achieve excellent stereocontrol in complex molecule synthesis, making it valuable in pharmaceutical and fine chemical industries. Its application extends to the preparation of bioactive molecules and intermediates where precise chirality is critical for biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿2,150.00
inventory 25mg
10-20 days ฿7,920.00
inventory 100mg
10-20 days ฿30,720.00

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[S(R)]-N-[(R)-[(3-(Benzyloxy)-2-(dicyclohexylphosphino)phenyl)phenylmethyl]-2-methyl-2-propanesulfinamide
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Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations, particularly in rhodium- or ruthenium-catalyzed asymmetric hydrogenation reactions. It is especially effective in the synthesis of chiral amines, amino acids, and other nitrogen-containing compounds where high enantiomeric excess is required. Due to its rigid, sterically demanding structure and well-defined stereochemistry, it helps achieve excellent stereocontrol in complex molecul

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations, particularly in rhodium- or ruthenium-catalyzed asymmetric hydrogenation reactions. It is especially effective in the synthesis of chiral amines, amino acids, and other nitrogen-containing compounds where high enantiomeric excess is required. Due to its rigid, sterically demanding structure and well-defined stereochemistry, it helps achieve excellent stereocontrol in complex molecule synthesis, making it valuable in pharmaceutical and fine chemical industries. Its application extends to the preparation of bioactive molecules and intermediates where precise chirality is critical for biological activity.

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