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

98%

Reagent Code: #70394
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CAS Number 141977-92-6

science Other reagents with same CAS 141977-92-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 326.39 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

description Product Description

Used in asymmetric synthesis as a chiral ligand or catalyst, enabling the production of enantiomerically pure compounds in pharmaceutical and fine chemical industries. It plays a role in facilitating stereoselective reactions, such as hydrogenation or carbon-carbon bond formation, which are critical in drug development. Its binaphthyl backbone provides structural rigidity, enhancing selectivity in catalytic processes. Additionally, it is employed in the synthesis of complex natural products and bioactive molecules, contributing to advancements in medicinal chemistry.

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Test Parameter Specification
Appearance solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,680.00

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N-[(1R)-2'-aMino[1,1'-binaphthalen]-2-yl]-AcetaMide
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Used in asymmetric synthesis as a chiral ligand or catalyst, enabling the production of enantiomerically pure compounds in pharmaceutical and fine chemical industries. It plays a role in facilitating stereoselective reactions, such as hydrogenation or carbon-carbon bond formation, which are critical in drug development. Its binaphthyl backbone provides structural rigidity, enhancing selectivity in catalytic processes. Additionally, it is employed in the synthesis of complex natural products and bioactive

Used in asymmetric synthesis as a chiral ligand or catalyst, enabling the production of enantiomerically pure compounds in pharmaceutical and fine chemical industries. It plays a role in facilitating stereoselective reactions, such as hydrogenation or carbon-carbon bond formation, which are critical in drug development. Its binaphthyl backbone provides structural rigidity, enhancing selectivity in catalytic processes. Additionally, it is employed in the synthesis of complex natural products and bioactive molecules, contributing to advancements in medicinal chemistry.

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