(11bS)-2,6-Bis[3,5-bis(trifluoromethyl)phenyl]-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin

98%

Reagent Code: #70532
fingerprint
CAS Number 878111-17-2

science Other reagents with same CAS 878111-17-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 772.5 g/mol
Formula C₃₆H₁₇F₁₂O₄P
thermostat Physical Properties
Melting Point 171-177°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Enhances enantioselectivity in processes such as hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. Valuable in pharmaceutical synthesis for producing enantiomerically pure compounds. Also employed in organic synthesis to achieve high selectivity and efficiency in complex molecule construction. Its unique structure and steric properties make it suitable for challenging catalytic applications.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White Powder
Purity (%) 97.5-100
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,228.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(11bS)-2,6-Bis[3,5-bis(trifluoromethyl)phenyl]-4-hydroxy-4-oxide-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin
No image available

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Enhances enantioselectivity in processes such as hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. Valuable in pharmaceutical synthesis for producing enantiomerically pure compounds. Also employed in organic synthesis to achieve high selectivity and efficiency in complex molecule construction. Its unique structure and steric properties make it suitable for challengin

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Enhances enantioselectivity in processes such as hydrogenation, carbon-carbon bond formation, and other stereospecific transformations. Valuable in pharmaceutical synthesis for producing enantiomerically pure compounds. Also employed in organic synthesis to achieve high selectivity and efficiency in complex molecule construction. Its unique structure and steric properties make it suitable for challenging catalytic applications.

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...