(4S,4'S)-4,4'-Di-sec-butyl-4,4',5,5'-tetrahydro-2,2'-bioxazole

98%

Reagent Code: #236869
fingerprint
CAS Number 2374958-89-9

science Other reagents with same CAS 2374958-89-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.35 g/mol
Formula C₁₄H₂₄N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid oxazoline framework enhances stereocontrol, making it effective in reactions such as asymmetric allylic alkylation, Diels-Alder cycloadditions, and copper-catalyzed conjugate additions. The sec-butyl groups contribute to high enantioselectivity by creating a well-defined chiral environment around the metal center. Commonly employed with transition metals like copper, palladium, or nickel to achieve high yields and excellent ee values in the synthesis of chiral building blocks for pharmaceuticals and fine chemicals.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,720.00
inventory 250mg
10-20 days ฿16,950.00
inventory 1g
10-20 days ฿34,530.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(4S,4'S)-4,4'-Di-sec-butyl-4,4',5,5'-tetrahydro-2,2'-bioxazole
No image available

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid oxazoline framework enhances stereocontrol, making it effective in reactions such as asymmetric allylic alkylation, Diels-Alder cycloadditions, and copper-catalyzed conjugate additions. The sec-butyl groups contribute to high enantioselectivity by creating a well-defined chiral environment around the metal center. Commonly employed with transition metals like copper, palladium, or nickel t

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid oxazoline framework enhances stereocontrol, making it effective in reactions such as asymmetric allylic alkylation, Diels-Alder cycloadditions, and copper-catalyzed conjugate additions. The sec-butyl groups contribute to high enantioselectivity by creating a well-defined chiral environment around the metal center. Commonly employed with transition metals like copper, palladium, or nickel to achieve high yields and excellent ee values in the synthesis of chiral building blocks 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...