(R)-2-(6-(Dicyclopentylmethyl)pyridin-2-yl)-4-phenyl-4,5-dihydrooxazole

97%

Reagent Code: #231851
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CAS Number 2417528-07-3

science Other reagents with same CAS 2417528-07-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 374.52 g/mol
Formula C₂₅H₃₀N₂O
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 rigid oxazole backbone and stereogenic center make it effective in controlling stereochemistry during carbon–carbon bond-forming reactions, particularly in transition metal-catalyzed transformations. Commonly applied in pharmaceutical research for developing chiral intermediates where high enantioselectivity is required. Also employed in the design of catalysts for hydrogenation and cross-coupling reactions due to its strong coordination ability with metals like palladium and rhodium.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿5,680.00
250mg
10-20 days ฿13,060.00
1g
10-20 days ฿45,700.00
(R)-2-(6-(Dicyclopentylmethyl)pyridin-2-yl)-4-phenyl-4,5-dihydrooxazole
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Used in asymmetric synthesis as a chiral auxiliary or ligand in catalytic reactions, enabling the formation of enantiomerically enriched compounds. Its rigid oxazole backbone and stereogenic center make it effective in controlling stereochemistry during carbon–carbon bond-forming reactions, particularly in transition metal-catalyzed transformations. Commonly applied in pharmaceutical research for developing chiral intermediates where high enantioselectivity is required. Also employed in the design of cat

Used in asymmetric synthesis as a chiral auxiliary or ligand in catalytic reactions, enabling the formation of enantiomerically enriched compounds. Its rigid oxazole backbone and stereogenic center make it effective in controlling stereochemistry during carbon–carbon bond-forming reactions, particularly in transition metal-catalyzed transformations. Commonly applied in pharmaceutical research for developing chiral intermediates where high enantioselectivity is required. Also employed in the design of catalysts for hydrogenation and cross-coupling reactions due to its strong coordination ability with metals like palladium and rhodium.

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