(R)-3,3'-Bis[4-tert-butylphenyl]-5,5',6,6',7,7',8,8'-octahydro-[1,1'-binaphthalene]-2,2'-diol

≥98%,99%e.e.

Reagent Code: #70357
fingerprint
CAS Number 1205537-80-9

science Other reagents with same CAS 1205537-80-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 558.8 g/mol
Formula C₄₀H₄₆O₂
thermostat Physical Properties
Melting Point 147 °C
Boiling Point 668.5±55.0 °C
inventory_2 Storage & Handling
Density 1.097±0.06 g/mL
Storage room temperature, dry

description Product Description

This chemical 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, carbon-carbon bond formation, and other stereoselective transformations. Its unique binaphthyl structure and tert-butylphenyl groups enhance its ability to induce chiral environments, making it valuable in the production of pharmaceuticals, fine chemicals, and agrochemicals where specific stereochemistry is critical. Additionally, it is used in the development of chiral catalysts for organic synthesis, contributing to advancements in the field of asymmetric catalysis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,080.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-3,3'-Bis[4-tert-butylphenyl]-5,5',6,6',7,7',8,8'-octahydro-[1,1'-binaphthalene]-2,2'-diol
No image available

This chemical 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, carbon-carbon bond formation, and other stereoselective transformations. Its unique binaphthyl structure and tert-butylphenyl groups enhance its ability to induce chiral environments, making it valuable in the production of pharmaceuticals, fine chemicals, and agro

This chemical 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, carbon-carbon bond formation, and other stereoselective transformations. Its unique binaphthyl structure and tert-butylphenyl groups enhance its ability to induce chiral environments, making it valuable in the production of pharmaceuticals, fine chemicals, and agrochemicals where specific stereochemistry is critical. Additionally, it is used in the development of chiral catalysts for organic synthesis, contributing to advancements in the field of asymmetric catalysis.

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...