(2R,5R)-2,5-Diphenylpyrrolidine

95%

Reagent Code: #70875
label
Alias (R,R)-2,5-Diphenylpyrrolidine
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CAS Number 155155-73-0

science Other reagents with same CAS 155155-73-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.32 g/mol
Formula C₁₆H₁₇N
badge Registry Numbers
EC Number 680-171-1
MDL Number MFCD07772441
thermostat Physical Properties
Melting Point 50 °C
Boiling Point 356.13 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.047±0.06 g/cm3
Storage 2-8°C, protected from light, sealed

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 stereochemistry makes it valuable in facilitating enantioselective reactions, particularly in the production of pharmaceuticals and fine chemicals. The compound is often employed in metal-catalyzed processes, such as hydrogenation or carbon-carbon bond formation, to achieve high enantiomeric purity in the final products. Additionally, its structural rigidity and ability to induce chirality make it a useful tool in the development of novel catalytic systems for organic synthesis. Researchers also explore its potential in creating chiral materials or as a building block for more complex molecular architectures.

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Test Parameter Specification
Melting point 46-53
Purity (GC) 95-100%
Specific Rotation [α]20/D (c=1, CHCl3) 105-113
Infrared Spectrometry Conforms to Structure
Note Low melting point solid; may change state in different environments (solid, liquid, or semi-solid)

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿29,448.00

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(2R,5R)-2,5-Diphenylpyrrolidine
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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 stereochemistry makes it valuable in facilitating enantioselective reactions, particularly in the production of pharmaceuticals and fine chemicals. The compound is often employed in metal-catalyzed processes, such as hydrogenation or carbon-carbon bond formation, to achieve high enantiomeric purity in the final products. Additionally, its structural rigidity and ability to

This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral ligand or catalyst. Its unique stereochemistry makes it valuable in facilitating enantioselective reactions, particularly in the production of pharmaceuticals and fine chemicals. The compound is often employed in metal-catalyzed processes, such as hydrogenation or carbon-carbon bond formation, to achieve high enantiomeric purity in the final products. Additionally, its structural rigidity and ability to induce chirality make it a useful tool in the development of novel catalytic systems for organic synthesis. Researchers also explore its potential in creating chiral materials or as a building block for more complex molecular architectures.

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