(S)-N,N-Diisopropyldinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine

98%,99%ee

Reagent Code: #38610
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CAS Number 185449-85-8

science Other reagents with same CAS 185449-85-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 415.4600 g/mol
Formula C₂₆H₂₆NO₂P
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high enantiomeric purity. Its unique structure allows for effective coordination with metal centers, enhancing the selectivity and efficiency of the reaction. This makes it valuable in the pharmaceutical industry for synthesizing enantiopure drugs and intermediates. Additionally, it finds use in academic research for developing new asymmetric catalytic methodologies.

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Test Parameter Specification
Appearance Off-White Powder
Purity (%) 97.5-100%
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,026.00

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(S)-N,N-Diisopropyldinaphtho[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. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high enantiomeric purity. Its unique structure allows for effective coordination with metal centers, enhancing the selectivity and efficiency of the reaction. This makes it valuable in the pharmaceutical industry for synthesizing enantiop

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high enantiomeric purity. Its unique structure allows for effective coordination with metal centers, enhancing the selectivity and efficiency of the reaction. This makes it valuable in the pharmaceutical industry for synthesizing enantiopure drugs and intermediates. Additionally, it finds use in academic research for developing new asymmetric catalytic methodologies.

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