(S)-(Rp)-PPFA

98%

Reagent Code: #68679
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CAS Number 137695-36-4

science Other reagents with same CAS 137695-36-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 441.34 g/mol
Formula C₂₆H₂₈FeNp
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description Product Description

(S)-(Rp)-PPFA is a chiral ferrocene-based phosphine ligand used primarily in asymmetric catalysis within organic chemistry. It serves as a key reagent in transition-metal-catalyzed reactions, such as palladium-catalyzed cross-coupling processes (e.g., Suzuki-Miyaura and Heck reactions), where it imparts high enantioselectivity to produce chiral molecules. This specialty chemical is invaluable for synthesizing enantiomerically pure compounds essential in pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure enables efficient chiral induction, facilitating the development of stereoselective synthetic methodologies and supporting advancements in drug discovery and material science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,195.00

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(S)-(Rp)-PPFA
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(S)-(Rp)-PPFA is a chiral ferrocene-based phosphine ligand used primarily in asymmetric catalysis within organic chemistry. It serves as a key reagent in transition-metal-catalyzed reactions, such as palladium-catalyzed cross-coupling processes (e.g., Suzuki-Miyaura and Heck reactions), where it imparts high enantioselectivity to produce chiral molecules. This specialty chemical is invaluable for synthesizing enantiomerically pure compounds essential in pharmaceuticals, agrochemicals, and fine chemicals.

(S)-(Rp)-PPFA is a chiral ferrocene-based phosphine ligand used primarily in asymmetric catalysis within organic chemistry. It serves as a key reagent in transition-metal-catalyzed reactions, such as palladium-catalyzed cross-coupling processes (e.g., Suzuki-Miyaura and Heck reactions), where it imparts high enantioselectivity to produce chiral molecules. This specialty chemical is invaluable for synthesizing enantiomerically pure compounds essential in pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure enables efficient chiral induction, facilitating the development of stereoselective synthetic methodologies and supporting advancements in drug discovery and material science.

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