[S(R)]-N-[(S)-(3,5-Di-tert-butyl-4-methoxyphenyl)[2-(di-tert-butylphosphino)phenyl]methyl]-2-methyl-2-propanesulfinamide

≥95%

Reagent Code: #68851
fingerprint
CAS Number 2565792-54-1

science Other reagents with same CAS 2565792-54-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 573.85 g/mol
Formula C₃₄H₅₆NO₂PS
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in asymmetric synthesis, particularly as a chiral ligand in transition metal-catalyzed reactions. Its unique structure, featuring tert-butyl groups and a sulfinamide moiety, makes it highly effective in inducing enantioselectivity in various organic transformations. It is commonly employed in the synthesis of complex molecules, including pharmaceuticals and fine chemicals, where precise control over stereochemistry is crucial. The compound’s sterically demanding and electron-rich environment enhances its ability to stabilize metal complexes, improving catalytic efficiency and selectivity. Additionally, it is used in the development of novel catalytic systems for C-C and C-X bond-forming reactions, contributing to advancements in synthetic organic chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,797.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
[S(R)]-N-[(S)-(3,5-Di-tert-butyl-4-methoxyphenyl)[2-(di-tert-butylphosphino)phenyl]methyl]-2-methyl-2-propanesulfinamide
No image available

This compound is primarily utilized in asymmetric synthesis, particularly as a chiral ligand in transition metal-catalyzed reactions. Its unique structure, featuring tert-butyl groups and a sulfinamide moiety, makes it highly effective in inducing enantioselectivity in various organic transformations. It is commonly employed in the synthesis of complex molecules, including pharmaceuticals and fine chemicals, where precise control over stereochemistry is crucial. The compound’s sterically demanding and el

This compound is primarily utilized in asymmetric synthesis, particularly as a chiral ligand in transition metal-catalyzed reactions. Its unique structure, featuring tert-butyl groups and a sulfinamide moiety, makes it highly effective in inducing enantioselectivity in various organic transformations. It is commonly employed in the synthesis of complex molecules, including pharmaceuticals and fine chemicals, where precise control over stereochemistry is crucial. The compound’s sterically demanding and electron-rich environment enhances its ability to stabilize metal complexes, improving catalytic efficiency and selectivity. Additionally, it is used in the development of novel catalytic systems for C-C and C-X bond-forming reactions, contributing to advancements in synthetic organic chemistry.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...