(1S)-N,N-Dimethyl-1-[(2R)-1',2-bis(diphenylphosphino)ferrocenyl]ethylamine

98%

Reagent Code: #38611
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CAS Number 119477-32-6

science Other reagents with same CAS 119477-32-6

blur_circular Chemical Specifications

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Weight 620.47 g/mol
Formula C₃₈H₃₂FeNP₂
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This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Its ferrocene backbone and diphenylphosphine groups provide excellent stability and selectivity, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its ability to induce high enantiomeric excess in products makes it a preferred choice for producing optically active compounds in industrial and academic research settings.

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inventory 50mg
10-20 days ฿2,232.00

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(1S)-N,N-Dimethyl-1-[(2R)-1',2-bis(diphenylphosphino)ferrocenyl]ethylamine
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This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Its ferrocene backbone and diphenylphosphine groups provide excellent stability and selectivity, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its ability to

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Its ferrocene backbone and diphenylphosphine groups provide excellent stability and selectivity, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, its ability to induce high enantiomeric excess in products makes it a preferred choice for producing optically active compounds in industrial and academic research settings.

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