(R)-()-2,2'-BIS(DICYCLOHEXYLPHOSPHINO)-1,1'-BINAPHTHYL

95%

Reagent Code: #68700
fingerprint
CAS Number 139139-92-7

science Other reagents with same CAS 139139-92-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 646.86 g/mol
Formula C₄₄H₅₆P₂
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a critical role in enantioselective hydrogenation, where it helps produce chiral molecules with high optical purity. Its application is prominent in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where achieving specific stereochemistry is essential. Additionally, it is utilized in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, to create complex organic compounds with high selectivity. Its robust structure and ability to induce chirality make it a valuable tool in organic synthesis and industrial processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,615.00
inventory 250mg
10-20 days ฿13,644.00
inventory 1g
10-20 days ฿52,911.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-()-2,2'-BIS(DICYCLOHEXYLPHOSPHINO)-1,1'-BINAPHTHYL
No image available

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a critical role in enantioselective hydrogenation, where it helps produce chiral molecules with high optical purity. Its application is prominent in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where achieving specific stereochemistry is essential. Additionally, it is utilized in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions,

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a critical role in enantioselective hydrogenation, where it helps produce chiral molecules with high optical purity. Its application is prominent in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where achieving specific stereochemistry is essential. Additionally, it is utilized in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, to create complex organic compounds with high selectivity. Its robust structure and ability to induce chirality make it a valuable tool in organic synthesis and industrial processes.

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...