BIS((R)-(-)-1-(1-NAPHTHYL)ETHYL)AMINE

≥95%

Reagent Code: #149522
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CAS Number 312619-39-9

science Other reagents with same CAS 312619-39-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 361.91 g/mol
Formula C₂₄H₂₄ClN
badge Registry Numbers
MDL Number MFCD00792501
thermostat Physical Properties
Melting Point 280 °C (dec.)(lit.)
Boiling Point 512.2 °C at 760mmHg
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral solvating agent and asymmetric synthesis auxiliary in organic chemistry. Its primary application lies in enantioselective reactions, where it helps induce chirality in newly formed molecules. Commonly employed in the development of chiral catalysts and ligands for transition metal-catalyzed reactions. Also utilized in NMR spectroscopy to differentiate enantiomers due to its ability to form diastereomeric complexes. Valuable in pharmaceutical research for synthesizing single-enantiomer compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,400.00
inventory 250mg
10-20 days ฿12,790.00

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BIS((R)-(-)-1-(1-NAPHTHYL)ETHYL)AMINE
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Used as a chiral solvating agent and asymmetric synthesis auxiliary in organic chemistry. Its primary application lies in enantioselective reactions, where it helps induce chirality in newly formed molecules. Commonly employed in the development of chiral catalysts and ligands for transition metal-catalyzed reactions. Also utilized in NMR spectroscopy to differentiate enantiomers due to its ability to form diastereomeric complexes. Valuable in pharmaceutical research for synthesizing single-enantiomer co

Used as a chiral solvating agent and asymmetric synthesis auxiliary in organic chemistry. Its primary application lies in enantioselective reactions, where it helps induce chirality in newly formed molecules. Commonly employed in the development of chiral catalysts and ligands for transition metal-catalyzed reactions. Also utilized in NMR spectroscopy to differentiate enantiomers due to its ability to form diastereomeric complexes. Valuable in pharmaceutical research for synthesizing single-enantiomer compounds.

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