3-(tert-Butyl)-4-(2,6-diisopropoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole

97%

Reagent Code: #153216
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CAS Number 2634687-76-4

science Other reagents with same CAS 2634687-76-4

blur_circular Chemical Specifications

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Weight 386.4642 g/mol
Formula C₂₃H₃₁O₃P
inventory_2 Storage & Handling
Storage 2-8°C, 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 steric bulk and electron-donating properties enhance enantioselectivity and reaction efficiency. Commonly employed in the synthesis of pharmaceuticals and fine chemicals where high optical purity is required. Effective in rhodium- and ruthenium-based catalytic systems for asymmetric hydrogenation of olefins and ketones. Also utilized in palladium-catalyzed transformations to control stereochemistry in complex molecule assembly.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,410.00
inventory 1g
10-20 days ฿20,700.00

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3-(tert-Butyl)-4-(2,6-diisopropoxyphenyl)-2,3-dihydrobenzo[d][1,3]oxaphosphole
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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 steric bulk and electron-donating properties enhance enantioselectivity and reaction efficiency. Commonly employed in the synthesis of pharmaceuticals and fine chemicals where high optical purity is required. Effective in rhodium- and ruthenium-based catalytic systems for asymmetric hydrogenation of olefins and ketones. Also utilized in palladium-catalyzed tr

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation and cross-coupling. Its steric bulk and electron-donating properties enhance enantioselectivity and reaction efficiency. Commonly employed in the synthesis of pharmaceuticals and fine chemicals where high optical purity is required. Effective in rhodium- and ruthenium-based catalytic systems for asymmetric hydrogenation of olefins and ketones. Also utilized in palladium-catalyzed transformations to control stereochemistry in complex molecule assembly.

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