(R)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-bis[4-(trifluoromethyl)phenyl]-[1,1'-binaphthalene]-2,2'-diol

≥95%,99%e.e.

Reagent Code: #70374
fingerprint
CAS Number 791616-69-8

science Other reagents with same CAS 791616-69-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 582.6 g/mol
Formula C₃₄H₂₈F₆O₂
thermostat Physical Properties
Boiling Point 620.7±55.0 °C
inventory_2 Storage & Handling
Density 1.315±0.06 g/mL
Storage room temperature, dry

description Product Description

This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce enantiomerically pure compounds. Its robust structure and ability to form stable complexes with metals make it valuable in pharmaceutical synthesis, where precise stereochemistry is crucial for drug efficacy. Additionally, it finds applications in the development of advanced materials and as a component in chiral catalysts for organic transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,400.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-bis[4-(trifluoromethyl)phenyl]-[1,1'-binaphthalene]-2,2'-diol
No image available

This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce enantiomerically pure compounds. Its robust structure and ability to form stable complexes with metals make it valuable in pharmaceutical synthesis, where precise stereochemistry is crucial for drug efficacy. Additionally, it finds applications in the de

This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce enantiomerically pure compounds. Its robust structure and ability to form stable complexes with metals make it valuable in pharmaceutical synthesis, where precise stereochemistry is crucial for drug efficacy. Additionally, it finds applications in the development of advanced materials and as a component in chiral catalysts for organic transformations.

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...