S-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: #68599
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CAS Number 712352-04-0

science Other reagents with same CAS 712352-04-0

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 in asymmetric synthesis, particularly in catalytic processes where enantioselectivity is crucial. It serves as a chiral ligand in transition metal catalysis, enabling the production of enantiomerically pure compounds. This is especially valuable in the pharmaceutical industry for the synthesis of chiral drugs, where the specific enantiomer often determines the drug's efficacy and safety. Additionally, it is employed in organic chemistry research to explore new methodologies for constructing complex molecular architectures with high stereochemical control. Its application extends to the development of advanced materials and fine chemicals, where precise stereochemistry is essential for desired properties and performance.

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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 ฿6,813.00

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S-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 in asymmetric synthesis, particularly in catalytic processes where enantioselectivity is crucial. It serves as a chiral ligand in transition metal catalysis, enabling the production of enantiomerically pure compounds. This is especially valuable in the pharmaceutical industry for the synthesis of chiral drugs, where the specific enantiomer often determines the drug's efficacy and safety. Additionally, it is employed in organic chemistry research to explore new methodol

This chemical is primarily utilized in asymmetric synthesis, particularly in catalytic processes where enantioselectivity is crucial. It serves as a chiral ligand in transition metal catalysis, enabling the production of enantiomerically pure compounds. This is especially valuable in the pharmaceutical industry for the synthesis of chiral drugs, where the specific enantiomer often determines the drug's efficacy and safety. Additionally, it is employed in organic chemistry research to explore new methodologies for constructing complex molecular architectures with high stereochemical control. Its application extends to the development of advanced materials and fine chemicals, where precise stereochemistry is essential for desired properties and performance.

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