(11bR)-2,6-Diphenyl-N,N-bis[(1R)-1-phenylethyl]dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine

97%

Reagent Code: #68587
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CAS Number 1204207-84-0

science Other reagents with same CAS 1204207-84-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 691.79 g/mol
Formula C₄₈H₃₈NO₂P
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. Its unique structure allows it to coordinate with metal centers, forming complexes that facilitate the production of chiral molecules with high optical purity. It is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other transition metal-catalyzed processes. The compound’s effectiveness in inducing chirality makes it valuable in the pharmaceutical industry for synthesizing enantiomerically pure drugs and intermediates. Additionally, it finds application in academic research for developing new catalytic methodologies and studying stereochemical outcomes in organic reactions.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿11,277.00

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(11bR)-2,6-Diphenyl-N,N-bis[(1R)-1-phenylethyl]dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine
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This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. Its unique structure allows it to coordinate with metal centers, forming complexes that facilitate the production of chiral molecules with high optical purity. It is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other transition metal-catalyzed processes. The compound’s effectiveness in inducing chirality makes it valuable

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. Its unique structure allows it to coordinate with metal centers, forming complexes that facilitate the production of chiral molecules with high optical purity. It is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other transition metal-catalyzed processes. The compound’s effectiveness in inducing chirality makes it valuable in the pharmaceutical industry for synthesizing enantiomerically pure drugs and intermediates. Additionally, it finds application in academic research for developing new catalytic methodologies and studying stereochemical outcomes in organic reactions.

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