(S)-4-Cyclohexyl-2-(pyridin-2-yl)-4,5-dihydrooxazole

98%,99%ee

Reagent Code: #38529
fingerprint
CAS Number 192318-04-0

science Other reagents with same CAS 192318-04-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.3055 g/mol
Formula C₁₄H₁₈N₂O
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand in catalytic reactions. Its structure, featuring a dihydrooxazole ring and a pyridine moiety, makes it effective in coordinating with metal centers, particularly in transition metal-catalyzed processes. It is often employed in enantioselective transformations, such as hydrogenation and carbon-carbon bond-forming reactions, to produce chiral molecules with high optical purity. Additionally, it finds application in the development of pharmaceuticals and fine chemicals, where precise control over stereochemistry is crucial. Its stability and ability to induce high enantioselectivity make it a valuable tool in organic synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,646.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-4-Cyclohexyl-2-(pyridin-2-yl)-4,5-dihydrooxazole
No image available

This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand in catalytic reactions. Its structure, featuring a dihydrooxazole ring and a pyridine moiety, makes it effective in coordinating with metal centers, particularly in transition metal-catalyzed processes. It is often employed in enantioselective transformations, such as hydrogenation and carbon-carbon bond-forming reactions, to produce chiral molecules with high optical purity. Additionally, it find

This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand in catalytic reactions. Its structure, featuring a dihydrooxazole ring and a pyridine moiety, makes it effective in coordinating with metal centers, particularly in transition metal-catalyzed processes. It is often employed in enantioselective transformations, such as hydrogenation and carbon-carbon bond-forming reactions, to produce chiral molecules with high optical purity. Additionally, it finds application in the development of pharmaceuticals and fine chemicals, where precise control over stereochemistry is crucial. Its stability and ability to induce high enantioselectivity make it a valuable tool in organic synthesis.

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...