(S)-1-[(S)-2-(Dicyclohexylphosphino)-ferrocenyl]ethyldicyclohexylphosphine

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Reagent Code: #37960
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CAS Number 246231-77-6

science Other reagents with same CAS 246231-77-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 606.6400 g/mol
Formula C₃₆H₅₆FeP₂
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MDL Number MFCD00800279
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Its effectiveness stems from its ability to induce high enantiomeric excess in the final products, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. The ferrocene backbone and dicyclohexylphosphine groups provide stability and steric control, enhancing the selectivity and efficiency of catalytic processes. Its application is particularly prominent in the production of chiral intermediates for drugs and bioactive molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,110.00
inventory 250mg
10-20 days ฿2,100.00
inventory 1g
10-20 days ฿7,650.00
inventory 5g
10-20 days ฿38,210.00

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(S)-1-[(S)-2-(Dicyclohexylphosphino)-ferrocenyl]ethyldicyclohexylphosphine
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This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Its effectiveness stems from its ability to induce high enantiomeric excess in the final products, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. The ferrocene backbone and di

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Its effectiveness stems from its ability to induce high enantiomeric excess in the final products, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. The ferrocene backbone and dicyclohexylphosphine groups provide stability and steric control, enhancing the selectivity and efficiency of catalytic processes. Its application is particularly prominent in the production of chiral intermediates for drugs and bioactive molecules.

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