(S)-6,6'-Bis(3,5-dichlorophenyl)-2,2',3,3'-tetrahydro-1,1'-spirobi[indene]-7,7'-diol

≥98%,≥99%e.e.

Reagent Code: #65663

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 542.3 g/mol
Formula C₂₉H₂₀Cl₄O₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the field of asymmetric catalysis, where it serves as a chiral ligand. Its unique structure, featuring a spirobi[indene] core and dichlorophenyl groups, enables it to effectively induce chirality in various catalytic reactions, particularly in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. Additionally, its stability and steric properties make it suitable for use in complex organic transformations, such as hydrogenation and carbon-carbon bond-forming reactions, where high enantioselectivity is crucial. The compound’s ability to form stable complexes with transition metals further enhances its utility in catalytic systems.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿35,469.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-6,6'-Bis(3,5-dichlorophenyl)-2,2',3,3'-tetrahydro-1,1'-spirobi[indene]-7,7'-diol
No image available

This compound is primarily utilized in the field of asymmetric catalysis, where it serves as a chiral ligand. Its unique structure, featuring a spirobi[indene] core and dichlorophenyl groups, enables it to effectively induce chirality in various catalytic reactions, particularly in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. Additionally, its stability and steric properties make it suitable for use in complex organic transformations, such as hydrogenation and carbon-carbon

This compound is primarily utilized in the field of asymmetric catalysis, where it serves as a chiral ligand. Its unique structure, featuring a spirobi[indene] core and dichlorophenyl groups, enables it to effectively induce chirality in various catalytic reactions, particularly in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. Additionally, its stability and steric properties make it suitable for use in complex organic transformations, such as hydrogenation and carbon-carbon bond-forming reactions, where high enantioselectivity is crucial. The compound’s ability to form stable complexes with transition metals further enhances its utility in catalytic systems.

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...