2'-Benzyl-2-hydroxy-3-(diphenylphosphino)-[1,1'-binaphthalene]

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Reagent Code: #68745
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CAS Number 1621627-50-6

science Other reagents with same CAS 1621627-50-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 544.62 g/mol
Formula C₃₉H₂₉OP
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MDL Number MFCD30833864
inventory_2 Storage & Handling
Storage room temperature, sealed, inert gas

description Product Description

This chemical is primarily utilized 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 unique structure, featuring a binaphthalene backbone and a diphenylphosphino group, allows it to effectively coordinate with metal centers, enhancing the selectivity and efficiency of the catalytic process. This makes it valuable in the synthesis of chiral intermediates and active pharmaceutical ingredients (APIs) in the pharmaceutical industry. Additionally, it is employed in academic research to develop new catalytic methodologies and explore asymmetric synthesis pathways.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,355.00

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2'-Benzyl-2-hydroxy-3-(diphenylphosphino)-[1,1'-binaphthalene]
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This chemical is primarily utilized 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 unique structure, featuring a binaphthalene backbone and a diphenylphosphino group, allows it to effectively coordinate with metal centers, enhancing the selectivity and efficiency of the catalytic process. T

This chemical is primarily utilized 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 unique structure, featuring a binaphthalene backbone and a diphenylphosphino group, allows it to effectively coordinate with metal centers, enhancing the selectivity and efficiency of the catalytic process. This makes it valuable in the synthesis of chiral intermediates and active pharmaceutical ingredients (APIs) in the pharmaceutical industry. Additionally, it is employed in academic research to develop new catalytic methodologies and explore asymmetric synthesis pathways.

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