(S)-2-(6-(Dicyclohexylmethyl)pyridin-2-yl)-4-phenyl-4,5-dihydrooxazole

97%

Reagent Code: #237482
fingerprint
CAS Number 2828438-50-0

science Other reagents with same CAS 2828438-50-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 402.57 g/mol
Formula C₂₇H₃₄N₂O
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used in asymmetric synthesis as a chiral auxiliary or ligand in catalytic reactions, enabling the formation of enantiomerically enriched compounds. Its oxazole core and stereogenic center make it valuable in developing pharmaceuticals and fine chemicals where stereocontrol is critical. Commonly applied in transition metal-catalyzed transformations, such as hydrogenation or cross-coupling reactions, to achieve high enantioselectivity. Also employed in the design of specialized catalysts for organic synthesis and medicinal chemistry research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,680.00
inventory 1g
10-20 days ฿53,040.00
inventory 250mg
10-20 days ฿18,140.00
(S)-2-(6-(Dicyclohexylmethyl)pyridin-2-yl)-4-phenyl-4,5-dihydrooxazole
No image available

Used in asymmetric synthesis as a chiral auxiliary or ligand in catalytic reactions, enabling the formation of enantiomerically enriched compounds. Its oxazole core and stereogenic center make it valuable in developing pharmaceuticals and fine chemicals where stereocontrol is critical. Commonly applied in transition metal-catalyzed transformations, such as hydrogenation or cross-coupling reactions, to achieve high enantioselectivity. Also employed in the design of specialized catalysts for organic synthe

Used in asymmetric synthesis as a chiral auxiliary or ligand in catalytic reactions, enabling the formation of enantiomerically enriched compounds. Its oxazole core and stereogenic center make it valuable in developing pharmaceuticals and fine chemicals where stereocontrol is critical. Commonly applied in transition metal-catalyzed transformations, such as hydrogenation or cross-coupling reactions, to achieve high enantioselectivity. Also employed in the design of specialized catalysts for organic synthesis and medicinal chemistry research.

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...