N-[(1S)-2'-aMino[1,1'-binaphthalen]-2-yl]-AcetaMide

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Reagent Code: #65668
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CAS Number 35216-74-1

science Other reagents with same CAS 35216-74-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 326.39112 g/mol
Formula C₂₂H₁₈N₂O
thermostat Physical Properties
Melting Point 240-241 °C
Boiling Point 535.6±35.0 °C
inventory_2 Storage & Handling
Density 1.263±0.06 g/cm3
Storage 2-8°C, away from light

description Product Description

This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand or catalyst. Its unique structure, derived from binaphthyl, allows it to induce chirality in various organic reactions, making it valuable for producing enantiomerically pure compounds. It is often employed in transition metal-catalyzed reactions, such as asymmetric hydrogenation or carbon-carbon bond-forming reactions, which are critical in the synthesis of pharmaceuticals and fine chemicals. Additionally, its application extends to the development of chiral sensors or materials, where its ability to differentiate between enantiomers is leveraged for analytical purposes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,020.00

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N-[(1S)-2'-aMino[1,1'-binaphthalen]-2-yl]-AcetaMide
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This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand or catalyst. Its unique structure, derived from binaphthyl, allows it to induce chirality in various organic reactions, making it valuable for producing enantiomerically pure compounds. It is often employed in transition metal-catalyzed reactions, such as asymmetric hydrogenation or carbon-carbon bond-forming reactions, which are critical in the synthesis of pharmaceuticals and fine chemicals. Add

This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand or catalyst. Its unique structure, derived from binaphthyl, allows it to induce chirality in various organic reactions, making it valuable for producing enantiomerically pure compounds. It is often employed in transition metal-catalyzed reactions, such as asymmetric hydrogenation or carbon-carbon bond-forming reactions, which are critical in the synthesis of pharmaceuticals and fine chemicals. Additionally, its application extends to the development of chiral sensors or materials, where its ability to differentiate between enantiomers is leveraged for analytical purposes.

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