N-[(1R)-2'-amino-4,4',6,6'-tetrakis(trifluoromethyl)[1,1'-biphenyl]-2-yl]-P,P-diphenyl-Phosphinous amide

98%

Reagent Code: #70678
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CAS Number 1165709-81-8

science Other reagents with same CAS 1165709-81-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 640.4025794 g/mol
Formula C₂₈H₁₇F₁₂N₂P
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand in asymmetric catalysis. It plays a crucial role in facilitating enantioselective reactions, which are essential for producing optically active compounds in pharmaceuticals and fine chemicals. Its unique structure, featuring trifluoromethyl groups and a biphenyl backbone, enhances its stability and efficiency in catalytic processes. Additionally, it is employed in the development of novel catalytic systems for complex organic transformations, contributing to advancements in drug discovery and material science.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿2,925.00
inventory 50mg
10-20 days ฿11,700.00

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N-[(1R)-2'-amino-4,4',6,6'-tetrakis(trifluoromethyl)[1,1'-biphenyl]-2-yl]-P,P-diphenyl-Phosphinous amide
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This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand in asymmetric catalysis. It plays a crucial role in facilitating enantioselective reactions, which are essential for producing optically active compounds in pharmaceuticals and fine chemicals. Its unique structure, featuring trifluoromethyl groups and a biphenyl backbone, enhances its stability and efficiency in catalytic processes. Additionally, it is employed in the development of novel catalytic syst

This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand in asymmetric catalysis. It plays a crucial role in facilitating enantioselective reactions, which are essential for producing optically active compounds in pharmaceuticals and fine chemicals. Its unique structure, featuring trifluoromethyl groups and a biphenyl backbone, enhances its stability and efficiency in catalytic processes. Additionally, it is employed in the development of novel catalytic systems for complex organic transformations, contributing to advancements in drug discovery and material science.

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