(4S,4'S)-2,2'-(1-Phenylpropane-2,2-diyl)bis(4-isopropyl-4,5-dihydrooxazole)

97%

Reagent Code: #237008
fingerprint
CAS Number 698350-53-7

science Other reagents with same CAS 698350-53-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 342.48 g/mol
Formula C₂₁H₃₀N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. It forms complexes with transition metals like copper or nickel, enabling highly stereoselective carbon-carbon bond-forming reactions. Commonly applied in catalytic asymmetric alkylation and cyclopropanation reactions, where it helps achieve high enantiomeric excess. Its rigid, bidentate structure enhances stereocontrol, making it valuable in the synthesis of chiral intermediates for pharmaceuticals and fine chemicals.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,480.00
inventory 250mg
10-20 days ฿8,640.00
inventory 1g
10-20 days ฿30,010.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(4S,4'S)-2,2'-(1-Phenylpropane-2,2-diyl)bis(4-isopropyl-4,5-dihydrooxazole)
No image available

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. It forms complexes with transition metals like copper or nickel, enabling highly stereoselective carbon-carbon bond-forming reactions. Commonly applied in catalytic asymmetric alkylation and cyclopropanation reactions, where it helps achieve high enantiomeric excess. Its rigid, bidentate structure enhances stereocontrol, making it valuable in the synthesis of chiral intermediates for pharmaceuticals

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. It forms complexes with transition metals like copper or nickel, enabling highly stereoselective carbon-carbon bond-forming reactions. Commonly applied in catalytic asymmetric alkylation and cyclopropanation reactions, where it helps achieve high enantiomeric excess. Its rigid, bidentate structure enhances stereocontrol, making it valuable in the synthesis of chiral intermediates for pharmaceuticals and fine chemicals.

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...