(R)-N,N'-[1,1'-Binaphthalene]-2,2'-diylbis[2-(diphenylphosphino)benzamide]

≥95%,≥99%e.e.

Reagent Code: #70395
fingerprint
CAS Number 298695-62-2

science Other reagents with same CAS 298695-62-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 860.9 g/mol
Formula C₅₈H₄₂N₂O₂P₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other organic synthesis processes. Its binaphthyl backbone and phosphine groups enhance its ability to induce high enantioselectivity, making it valuable in the production of pharmaceuticals, fine chemicals, and agrochemicals where precise stereochemistry is essential. Additionally, its stability and efficiency in catalytic systems contribute to its use in research and industrial applications aimed at developing novel chiral compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,250.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-N,N'-[1,1'-Binaphthalene]-2,2'-diylbis[2-(diphenylphosphino)benzamide]
No image available

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other organic synthesis processes. Its binaphthyl backbone and phosphine groups enhance its ability to induce high enantioselectivity, making it valuable in the production of pharmaceuticals, fine chemicals, and agrochemicals where precise ster

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other organic synthesis processes. Its binaphthyl backbone and phosphine groups enhance its ability to induce high enantioselectivity, making it valuable in the production of pharmaceuticals, fine chemicals, and agrochemicals where precise stereochemistry is essential. Additionally, its stability and efficiency in catalytic systems contribute to its use in research and industrial applications aimed at developing novel chiral compounds.

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...