(R)-2-(2-(Diphenylphosphanyl)phenyl)-4-isopropyl-5,5-diphenyl-4,5-dihydrooxazole

98%

Reagent Code: #231284
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CAS Number 1904575-43-4

science Other reagents with same CAS 1904575-43-4

blur_circular Chemical Specifications

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Weight 525.62 g/mol
Formula C₃₆H₃₂NOP
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation and cross-coupling. Its structure enables high enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly coordinates with rhodium, ruthenium, or palladium to form catalysts that efficiently produce single-enantiomer products. Widely applied in academic and industrial research for developing stereoselective synthetic routes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,310.00
inventory 250mg
10-20 days ฿16,690.00
inventory 1g
10-20 days ฿53,860.00

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(R)-2-(2-(Diphenylphosphanyl)phenyl)-4-isopropyl-5,5-diphenyl-4,5-dihydrooxazole
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Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation and cross-coupling. Its structure enables high enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly coordinates with rhodium, ruthenium, or palladium to form catalysts that efficiently produce single-enantiomer products. Widely applied in academic and industrial research for developing stereoselective synthetic rout

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation and cross-coupling. Its structure enables high enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly coordinates with rhodium, ruthenium, or palladium to form catalysts that efficiently produce single-enantiomer products. Widely applied in academic and industrial research for developing stereoselective synthetic routes.

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