R-N-Methyl-N-[(1S)-1-phenylethyl]-Dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-aMine

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Reagent Code: #68593
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CAS Number 874221-90-6

science Other reagents with same CAS 874221-90-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 449.48 g/mol
Formula C₂₉H₂₄NO₂P
inventory_2 Storage & Handling
Storage room temperature, dry

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 the formation of carbon-carbon and carbon-heteroatom bonds, enhancing the efficiency and selectivity of the process. Its unique structure allows it to coordinate effectively with transition metals, making it valuable in asymmetric hydrogenation and other stereospecific transformations. Additionally, it finds application in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals, where precise control over stereochemistry is essential. Its role in these processes contributes to the development of more efficient and sustainable synthetic routes.

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Test Parameter Specification
Purity 97.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,100.00

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R-N-Methyl-N-[(1S)-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. It is often employed in the formation of carbon-carbon and carbon-heteroatom bonds, enhancing the efficiency and selectivity of the process. Its unique structure allows it to coordinate effectively with transition metals, making it valuable in asymmetric hydrogenation and other stereospecific transformations. Additionally, it finds application in the syn

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 the formation of carbon-carbon and carbon-heteroatom bonds, enhancing the efficiency and selectivity of the process. Its unique structure allows it to coordinate effectively with transition metals, making it valuable in asymmetric hydrogenation and other stereospecific transformations. Additionally, it finds application in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals, where precise control over stereochemistry is essential. Its role in these processes contributes to the development of more efficient and sustainable synthetic routes.

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