N-[(1S,2S)-2-Amino-1,2-diphenylethyl]-2,3,4,5,6-pentafluorobenzenesulfonamide

≥98%

Reagent Code: #71241
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CAS Number 313342-24-4

science Other reagents with same CAS 313342-24-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 442.4 g/mol
Formula C₂₀H₁₅F₅N₂O₂S
thermostat Physical Properties
Melting Point 196-198°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the field of asymmetric synthesis and catalysis. It serves as a chiral ligand or catalyst in various organic reactions, particularly in the synthesis of enantiomerically pure compounds. Its unique structure, featuring a pentafluorobenzenesulfonamide group and a chiral diamine backbone, makes it effective in inducing high enantioselectivity in reactions such as hydrogenations, aldol additions, and other carbon-carbon bond-forming processes. Additionally, it is employed in pharmaceutical research for the development of chiral drugs, where precise control over stereochemistry is crucial for efficacy and safety. Its robust and versatile nature also makes it suitable for use in material science, particularly in the design of chiral polymers or supramolecular assemblies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,680.00

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N-[(1S,2S)-2-Amino-1,2-diphenylethyl]-2,3,4,5,6-pentafluorobenzenesulfonamide
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This compound is primarily utilized in the field of asymmetric synthesis and catalysis. It serves as a chiral ligand or catalyst in various organic reactions, particularly in the synthesis of enantiomerically pure compounds. Its unique structure, featuring a pentafluorobenzenesulfonamide group and a chiral diamine backbone, makes it effective in inducing high enantioselectivity in reactions such as hydrogenations, aldol additions, and other carbon-carbon bond-forming processes. Additionally, it is employ

This compound is primarily utilized in the field of asymmetric synthesis and catalysis. It serves as a chiral ligand or catalyst in various organic reactions, particularly in the synthesis of enantiomerically pure compounds. Its unique structure, featuring a pentafluorobenzenesulfonamide group and a chiral diamine backbone, makes it effective in inducing high enantioselectivity in reactions such as hydrogenations, aldol additions, and other carbon-carbon bond-forming processes. Additionally, it is employed in pharmaceutical research for the development of chiral drugs, where precise control over stereochemistry is crucial for efficacy and safety. Its robust and versatile nature also makes it suitable for use in material science, particularly in the design of chiral polymers or supramolecular assemblies.

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