Bis((R)-4-methyl-4,5-dihydrooxazol-2-yl)methane

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Reagent Code: #153237
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CAS Number 2757082-29-2

science Other reagents with same CAS 2757082-29-2

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inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its structure enables coordination with transition metals, forming catalysts that promote high stereoselectivity in reactions such as hydrogenation, epoxidation, and cyclopropanation. Commonly applied in the synthesis of pharmaceutical intermediates and fine chemicals where control of stereochemistry is critical. Its effectiveness in metal-catalyzed reactions makes it valuable in academic and industrial research for developing efficient asymmetric synthetic routes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,860.00
inventory 250mg
10-20 days ฿10,050.00
inventory 1g
10-20 days ฿25,150.00
inventory 5g
10-20 days ฿93,240.00

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Bis((R)-4-methyl-4,5-dihydrooxazol-2-yl)methane
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its structure enables coordination with transition metals, forming catalysts that promote high stereoselectivity in reactions such as hydrogenation, epoxidation, and cyclopropanation. Commonly applied in the synthesis of pharmaceutical intermediates and fine chemicals where control of stereochemistry is critical. Its effectiveness in metal-catalyzed reactions makes it valuable in academic and indust

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its structure enables coordination with transition metals, forming catalysts that promote high stereoselectivity in reactions such as hydrogenation, epoxidation, and cyclopropanation. Commonly applied in the synthesis of pharmaceutical intermediates and fine chemicals where control of stereochemistry is critical. Its effectiveness in metal-catalyzed reactions makes it valuable in academic and industrial research for developing efficient asymmetric synthetic routes.

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