N-[(1S,2S)-2-aMino-1,2-diphenylethyl]-BenzenesulfonaMide

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Reagent Code: #70721
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CAS Number 300345-91-9

science Other reagents with same CAS 300345-91-9

blur_circular Chemical Specifications

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Weight 352.45 g/mol
Formula C₂₀H₂₀N₂O₂S
inventory_2 Storage & Handling
Storage 2-8°C, away from light

description Product Description

This compound is primarily utilized in the field of asymmetric synthesis and catalysis. It serves as a chiral auxiliary or ligand in various organic reactions, enabling the production of enantiomerically pure compounds. Its structure, featuring a benzenesulfonamide group and chiral centers, makes it effective in controlling stereochemistry during reactions such as hydrogenation, alkylation, or cyclization. It is also employed in the development of pharmaceuticals, particularly in the synthesis of chiral drugs, where precise stereochemistry is crucial for biological activity. Additionally, it finds use in academic research for studying enantioselective transformations and developing new catalytic methodologies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,392.00
inventory 1g
10-20 days ฿13,014.00

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N-[(1S,2S)-2-aMino-1,2-diphenylethyl]-BenzenesulfonaMide
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This compound is primarily utilized in the field of asymmetric synthesis and catalysis. It serves as a chiral auxiliary or ligand in various organic reactions, enabling the production of enantiomerically pure compounds. Its structure, featuring a benzenesulfonamide group and chiral centers, makes it effective in controlling stereochemistry during reactions such as hydrogenation, alkylation, or cyclization. It is also employed in the development of pharmaceuticals, particularly in the synthesis of chiral

This compound is primarily utilized in the field of asymmetric synthesis and catalysis. It serves as a chiral auxiliary or ligand in various organic reactions, enabling the production of enantiomerically pure compounds. Its structure, featuring a benzenesulfonamide group and chiral centers, makes it effective in controlling stereochemistry during reactions such as hydrogenation, alkylation, or cyclization. It is also employed in the development of pharmaceuticals, particularly in the synthesis of chiral drugs, where precise stereochemistry is crucial for biological activity. Additionally, it finds use in academic research for studying enantioselective transformations and developing new catalytic methodologies.

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