(9S)-9-(9-phenanthrenyloxy)-Cinchonan-6'-ol

98%

Reagent Code: #70245
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CAS Number 761434-36-0

science Other reagents with same CAS 761434-36-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 486.6035 g/mol
Formula C₃₃H₃₀N₂O₂
badge Registry Numbers
MDL Number MFCD23704926
thermostat Physical Properties
Boiling Point 704.1±55.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in the field of asymmetric synthesis, particularly as a chiral catalyst or ligand in organic reactions. It is often employed in enantioselective transformations, where it helps in producing specific enantiomers of chiral molecules, which is crucial in the synthesis of pharmaceuticals and fine chemicals. Its structure, featuring a phenanthrene group, enhances its ability to induce stereoselectivity in various catalytic processes, such as asymmetric hydrogenation or carbon-carbon bond formation. Additionally, it finds application in the development of advanced materials and in research focused on understanding chiral induction mechanisms.

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Test Parameter Specification
Appearance Report Result
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿22,860.00
inventory 50mg
10-20 days ฿5,742.00

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(9S)-9-(9-phenanthrenyloxy)-Cinchonan-6'-ol
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This chemical is primarily utilized in the field of asymmetric synthesis, particularly as a chiral catalyst or ligand in organic reactions. It is often employed in enantioselective transformations, where it helps in producing specific enantiomers of chiral molecules, which is crucial in the synthesis of pharmaceuticals and fine chemicals. Its structure, featuring a phenanthrene group, enhances its ability to induce stereoselectivity in various catalytic processes, such as asymmetric hydrogenation or carb

This chemical is primarily utilized in the field of asymmetric synthesis, particularly as a chiral catalyst or ligand in organic reactions. It is often employed in enantioselective transformations, where it helps in producing specific enantiomers of chiral molecules, which is crucial in the synthesis of pharmaceuticals and fine chemicals. Its structure, featuring a phenanthrene group, enhances its ability to induce stereoselectivity in various catalytic processes, such as asymmetric hydrogenation or carbon-carbon bond formation. Additionally, it finds application in the development of advanced materials and in research focused on understanding chiral induction mechanisms.

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