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

≥98%,99%e.e.

Reagent Code: #70344
fingerprint
CAS Number 791616-67-6

science Other reagents with same CAS 791616-67-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 536.6 g/mol
Formula C₃₂H₂₈N₂O₆
thermostat Physical Properties
Boiling Point 727.9±60.0 °C
inventory_2 Storage & Handling
Density 1.343±0.06 g/mL
Storage room temperature, dry

description Product Description

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in enantioselective reactions, particularly in the formation of chiral molecules, which are crucial in the pharmaceutical industry for producing drugs with high stereochemical purity. Its structure allows it to effectively induce asymmetry in reactions like hydrogenation, oxidation, and carbon-carbon bond formation. Additionally, it is employed in the development of advanced materials and sensors, where its chiral properties enhance selectivity and performance.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,950.00
inventory 100mg
10-20 days ฿6,790.00

Cart

No products

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

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in enantioselective reactions, particularly in the formation of chiral molecules, which are crucial in the pharmaceutical industry for producing drugs with high stereochemical purity. Its structure allows it to effectively induce asymmetry in reactions like hydrogenation, oxidation, and carbon-carbon bond formation. Additionally, it is employed in the development of advanced materials a

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in enantioselective reactions, particularly in the formation of chiral molecules, which are crucial in the pharmaceutical industry for producing drugs with high stereochemical purity. Its structure allows it to effectively induce asymmetry in reactions like hydrogenation, oxidation, and carbon-carbon bond formation. Additionally, it is employed in the development of advanced materials and sensors, where its chiral properties enhance selectivity and performance.

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...