(11bS)-N,N-Bis[(R)-1-phenylethyl]-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine

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Reagent Code: #68598
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CAS Number 497883-22-4

science Other reagents with same CAS 497883-22-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 539.6 g/mol
Formula C₃₆H₃₀NO₂P
badge Registry Numbers
MDL Number MFCD08561138
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in organic synthesis. It plays a significant role in facilitating enantioselective reactions, such as hydrogenation, carbon-carbon bond formation, and other transformations where high stereocontrol is required. Its unique structure enables it to coordinate with metal centers, enhancing the selectivity and efficiency of catalytic processes. This makes it valuable in the pharmaceutical industry for the synthesis of chiral drugs and intermediates, where achieving specific enantiomers is crucial for biological activity. Additionally, it is employed in academic research to develop new methodologies in asymmetric synthesis.

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Test Parameter Specification
Appearance White to Off-White Powder
Purity 97.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,600.00
inventory 250mg
10-20 days ฿5,450.00

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(11bS)-N,N-Bis[(R)-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 catalysis, particularly in organic synthesis. It plays a significant role in facilitating enantioselective reactions, such as hydrogenation, carbon-carbon bond formation, and other transformations where high stereocontrol is required. Its unique structure enables it to coordinate with metal centers, enhancing the selectivity and efficiency of catalytic processes. This makes it valuable in the pharmaceutical industry for the synthesis of

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in organic synthesis. It plays a significant role in facilitating enantioselective reactions, such as hydrogenation, carbon-carbon bond formation, and other transformations where high stereocontrol is required. Its unique structure enables it to coordinate with metal centers, enhancing the selectivity and efficiency of catalytic processes. This makes it valuable in the pharmaceutical industry for the synthesis of chiral drugs and intermediates, where achieving specific enantiomers is crucial for biological activity. Additionally, it is employed in academic research to develop new methodologies in asymmetric synthesis.

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