(S)-N-(1-(2-(Anthracen-9-yl)phenyl)-2-(diphenylphosphanyl)ethyl)-3,5-bis(trifluoromethyl)benzamide

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Reagent Code: #236801
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CAS Number 2011787-22-5

science Other reagents with same CAS 2011787-22-5

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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 transition metal-catalyzed enantioselective reactions. Its structure enables high stereocontrol in hydrogenation and cross-coupling reactions, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. The anthracenyl and trifluoromethyl groups enhance ligand rigidity and electron-withdrawing properties, improving catalytic efficiency and enantioselectivity. Commonly applied in ruthenium- or rhodium-based catalytic systems for the production of chiral intermediates in drug development.

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inventory 25mg
10-20 days ฿5,070.00

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(S)-N-(1-(2-(Anthracen-9-yl)phenyl)-2-(diphenylphosphanyl)ethyl)-3,5-bis(trifluoromethyl)benzamide
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Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed enantioselective reactions. Its structure enables high stereocontrol in hydrogenation and cross-coupling reactions, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. The anthracenyl and trifluoromethyl groups enhance ligand rigidity and electron-withdrawing properties, improving catalytic efficiency and enantioselectivity. Commonly applied in ruthenium- or rhodium-based ca

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed enantioselective reactions. Its structure enables high stereocontrol in hydrogenation and cross-coupling reactions, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. The anthracenyl and trifluoromethyl groups enhance ligand rigidity and electron-withdrawing properties, improving catalytic efficiency and enantioselectivity. Commonly applied in ruthenium- or rhodium-based catalytic systems for the production of chiral intermediates in drug development.

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