(4R,5R)-4,5-Diphenyl-2-(6-phenylpyridin-2-yl)-4,5-dihydrooxazole

98%, 99%e.e.

Reagent Code: #231807
fingerprint
CAS Number 2757082-61-2

science Other reagents with same CAS 2757082-61-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 376.45 g/mol
Formula C₂₆H₂₀N₂O
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis of pharmaceutical intermediates. Its rigid oxazoline framework enhances stereocontrol in transition metal-catalyzed reactions such as hydrogenation and cyclopropanation. Commonly employed with palladium or copper complexes to achieve high enantiomeric excess in the formation of C–C and C–heteroatom bonds. Valued for its ability to induce chirality in the synthesis of bioactive molecules, including alpha-aryl carbonyl derivatives and nitrogen-containing heterocycles.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿7,750.00
250mg
10-20 days ฿11,670.00
1g
10-20 days ฿29,170.00
(4R,5R)-4,5-Diphenyl-2-(6-phenylpyridin-2-yl)-4,5-dihydrooxazole
No image available

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis of pharmaceutical intermediates. Its rigid oxazoline framework enhances stereocontrol in transition metal-catalyzed reactions such as hydrogenation and cyclopropanation. Commonly employed with palladium or copper complexes to achieve high enantiomeric excess in the formation of C–C and C–heteroatom bonds. Valued for its ability to induce chirality in the synthesis of bioactive molecules, including alpha-aryl carbo

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis of pharmaceutical intermediates. Its rigid oxazoline framework enhances stereocontrol in transition metal-catalyzed reactions such as hydrogenation and cyclopropanation. Commonly employed with palladium or copper complexes to achieve high enantiomeric excess in the formation of C–C and C–heteroatom bonds. Valued for its ability to induce chirality in the synthesis of bioactive molecules, including alpha-aryl carbonyl derivatives and nitrogen-containing heterocycles.

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...