N-[(1S)-1-[(Diphenylphosphino)Methyl]-2-Methylpropyl]-3,5-Bis(Trifluoromethyl)Benzamide

95%

Reagent Code: #220046
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CAS Number 1451091-01-2

science Other reagents with same CAS 1451091-01-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 511.44 g/mol
Formula C₂₆H₂₄F₆NOP
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation and cross-coupling. Its phosphine group coordinates effectively with metals like rhodium, ruthenium, and palladium, enabling high enantioselectivity in the synthesis of pharmaceutical intermediates and fine chemicals. The steric bulk and electron-withdrawing trifluoromethyl groups enhance catalytic efficiency and stereochemical control. Commonly applied in the development of active pharmaceutical ingredients where precise chirality is critical for biological activity.

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inventory 100mg
10-20 days ฿22,190.00

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N-[(1S)-1-[(Diphenylphosphino)Methyl]-2-Methylpropyl]-3,5-Bis(Trifluoromethyl)Benzamide
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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 phosphine group coordinates effectively with metals like rhodium, ruthenium, and palladium, enabling high enantioselectivity in the synthesis of pharmaceutical intermediates and fine chemicals. The steric bulk and electron-withdrawing trifluoromethyl groups enhance catalytic efficiency and stereochemical control. Commonly applied in the development of active

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation and cross-coupling. Its phosphine group coordinates effectively with metals like rhodium, ruthenium, and palladium, enabling high enantioselectivity in the synthesis of pharmaceutical intermediates and fine chemicals. The steric bulk and electron-withdrawing trifluoromethyl groups enhance catalytic efficiency and stereochemical control. Commonly applied in the development of active pharmaceutical ingredients where precise chirality is critical for biological activity.

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