R-N,N'-bis[[2-(diphenylphosphino)phenyl]Methyl]-[1,1'-Binaphthalene]-2,2'-diaMine

98%

Reagent Code: #70397
fingerprint
CAS Number 288093-09-4

science Other reagents with same CAS 288093-09-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 832.946762 g/mol
Formula C₅₈H₄₆N₂P₂
inventory_2 Storage & Handling
Storage 2-8°C, away from light

description Product Description

This chemical is widely utilized in the field of asymmetric catalysis, particularly in the synthesis of chiral compounds. It serves as a highly effective ligand in transition metal-catalyzed reactions, such as hydrogenation, cross-coupling, and allylic substitution. Its unique structure, featuring a binaphthyl backbone and phosphine groups, enables precise control over stereochemistry, making it invaluable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its application extends to the development of advanced materials, where it aids in creating chiral polymers and supramolecular assemblies with specific optical properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿9,180.00
inventory 100mg
10-20 days ฿27,900.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
R-N,N'-bis[[2-(diphenylphosphino)phenyl]Methyl]-[1,1'-Binaphthalene]-2,2'-diaMine
No image available

This chemical is widely utilized in the field of asymmetric catalysis, particularly in the synthesis of chiral compounds. It serves as a highly effective ligand in transition metal-catalyzed reactions, such as hydrogenation, cross-coupling, and allylic substitution. Its unique structure, featuring a binaphthyl backbone and phosphine groups, enables precise control over stereochemistry, making it invaluable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its applicat

This chemical is widely utilized in the field of asymmetric catalysis, particularly in the synthesis of chiral compounds. It serves as a highly effective ligand in transition metal-catalyzed reactions, such as hydrogenation, cross-coupling, and allylic substitution. Its unique structure, featuring a binaphthyl backbone and phosphine groups, enables precise control over stereochemistry, making it invaluable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its application extends to the development of advanced materials, where it aids in creating chiral polymers and supramolecular assemblies with specific optical properties.

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...