(R)-1-[(R)-2-[Bis[4-(trifluoromethyl)phenyl]phosphino]ferrocenyl]ethylbis[4-(trifluoromethyl)phenyl]phosphine

97%

Reagent Code: #37374
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CAS Number 166172-60-7

science Other reagents with same CAS 166172-60-7

blur_circular Chemical Specifications

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Weight 854.4200 g/mol
Formula C₄₀H₂₈F₁₂FeP₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring ferrocene and trifluoromethylphenyl groups, enhances stereoselectivity in processes such as hydrogenation, carbon-carbon bond formation, and other enantioselective transformations. It is especially effective in synthesizing pharmaceuticals and fine chemicals where high enantiomeric purity is critical. The trifluoromethyl groups improve the ligand's electron-withdrawing properties, making it suitable for reactions requiring precise control over reactivity and selectivity. Its application extends to industrial and academic research for developing advanced catalytic systems.

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inventory 100mg
10-20 days ฿2,448.00

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(R)-1-[(R)-2-[Bis[4-(trifluoromethyl)phenyl]phosphino]ferrocenyl]ethylbis[4-(trifluoromethyl)phenyl]phosphine
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring ferrocene and trifluoromethylphenyl groups, enhances stereoselectivity in processes such as hydrogenation, carbon-carbon bond formation, and other enantioselective transformations. It is especially effective in synthesizing pharmaceuticals and fine chemicals where high enantiomeric purity is critical. The trifluoromethyl groups improve the l

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring ferrocene and trifluoromethylphenyl groups, enhances stereoselectivity in processes such as hydrogenation, carbon-carbon bond formation, and other enantioselective transformations. It is especially effective in synthesizing pharmaceuticals and fine chemicals where high enantiomeric purity is critical. The trifluoromethyl groups improve the ligand's electron-withdrawing properties, making it suitable for reactions requiring precise control over reactivity and selectivity. Its application extends to industrial and academic research for developing advanced catalytic systems.

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