(S)-()-2,2'-Bis[di(3,5-di-i-propyl-4-dimethylaminophenyl)phosphino]-6,6'-dimethoxy-1,1'-biphenyl

98%

Reagent Code: #37802
fingerprint
CAS Number 919338-66-2

science Other reagents with same CAS 919338-66-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1091.5161 g/mol
Formula C₇₀H₁₀₀N₄O₂P₂
badge Registry Numbers
MDL Number MFCD09753010
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific processes. Its sterically demanding and electron-rich structure enhances selectivity and efficiency in producing chiral molecules, which are crucial in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its application extends to the development of advanced materials and catalysts for organic synthesis, where precise control over stereochemistry is essential.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,445.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-()-2,2'-Bis[di(3,5-di-i-propyl-4-dimethylaminophenyl)phosphino]-6,6'-dimethoxy-1,1'-biphenyl
No image available

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific processes. Its sterically demanding and electron-rich structure enhances selectivity and efficiency in producing chiral molecules, which are crucial in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Add

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific processes. Its sterically demanding and electron-rich structure enhances selectivity and efficiency in producing chiral molecules, which are crucial in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its application extends to the development of advanced materials and catalysts for organic synthesis, where precise control over stereochemistry is essential.

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...