(11bS)-4-Hydroxy-2,6-bis(4-(trifluoromethyl)phenyl)-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide

98%

Reagent Code: #236903
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CAS Number 2635339-84-1

science Other reagents with same CAS 2635339-84-1

blur_circular Chemical Specifications

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Weight 644.54 g/mol
Formula C₃₄H₂₇F₆O₄P
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 asymmetric hydrogenation and cross-coupling reactions. Its rigid, bidentate structure enables high enantioselectivity and catalytic efficiency. Commonly employed in the synthesis of pharmaceutical intermediates and fine chemicals where control of stereochemistry is critical. Shows particular effectiveness with rhodium and ruthenium complexes, facilitating the production of enantiomerically pure compounds in medicinal chemistry and agrochemical industries.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,890.00
inventory 250mg
10-20 days ฿7,160.00

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(11bS)-4-Hydroxy-2,6-bis(4-(trifluoromethyl)phenyl)-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide
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Used as a chiral ligand in asymmetric catalysis, particularly in transition-metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling reactions. Its rigid, bidentate structure enables high enantioselectivity and catalytic efficiency. Commonly employed in the synthesis of pharmaceutical intermediates and fine chemicals where control of stereochemistry is critical. Shows particular effectiveness with rhodium and ruthenium complexes, facilitating the production of enantiomerically pure c

Used as a chiral ligand in asymmetric catalysis, particularly in transition-metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling reactions. Its rigid, bidentate structure enables high enantioselectivity and catalytic efficiency. Commonly employed in the synthesis of pharmaceutical intermediates and fine chemicals where control of stereochemistry is critical. Shows particular effectiveness with rhodium and ruthenium complexes, facilitating the production of enantiomerically pure compounds in medicinal chemistry and agrochemical industries.

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