(S)-2,2'-Bis(diphenylphosphino)-4,4',6,6'-tetramethoxy)-1,1'-biphenyl

98%

Reagent Code: #37993
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CAS Number 1365531-76-5

science Other reagents with same CAS 1365531-76-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 642.6600 g/mol
Formula C₄₀H₃₆O₄P₂
badge Registry Numbers
MDL Number MFCD19443622
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. It plays a critical role in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its unique structure, featuring electron-rich phosphine groups and methoxy substituents, enhances its ability to coordinate with metals and induce high enantioselectivity in the synthesis of chiral molecules. This makes it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals where specific enantiomers are required for desired biological activity or performance. Its application is particularly prominent in the synthesis of complex organic compounds with high precision and efficiency.

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inventory 100mg
10-20 days ฿3,285.00

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(S)-2,2'-Bis(diphenylphosphino)-4,4',6,6'-tetramethoxy)-1,1'-biphenyl
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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 critical role in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its unique structure, featuring electron-rich phosphine groups and methoxy substituents, enhances its ability to coordinate with metals and induce high enantioselectivity in the synthesis of chiral molecules. This makes it va

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a critical role in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its unique structure, featuring electron-rich phosphine groups and methoxy substituents, enhances its ability to coordinate with metals and induce high enantioselectivity in the synthesis of chiral molecules. This makes it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals where specific enantiomers are required for desired biological activity or performance. Its application is particularly prominent in the synthesis of complex organic compounds with high precision and efficiency.

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