(4R,4'R)-2,2'-Cyclopropylidenebis[4,5-dihydro-4-phenylo xazole]

98%

Reagent Code: #59707
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CAS Number 1819994-24-5

science Other reagents with same CAS 1819994-24-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.3957 g/mol
Formula C₂₁H₂₀N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is effective in facilitating the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals and fine chemicals. Additionally, it is employed in transition metal-catalyzed reactions, such as hydrogenation and carbon-carbon bond formation, to enhance the efficiency and selectivity of the process. Its unique structure and stereochemistry contribute to its ability to control the spatial arrangement of atoms in the final product, ensuring high purity and desired optical activity.

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Test Parameter Specification
Appearance Yellow viscous liquid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿4,990.00
inventory 50mg
10-20 days ฿9,100.00

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(4R,4'R)-2,2'-Cyclopropylidenebis[4,5-dihydro-4-phenylo xazole]
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This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is effective in facilitating the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals and fine chemicals. Additionally, it is employed in transition metal-catalyzed reactions, such as hydrogenation and carbon-carbon bond formation, to enhance the efficiency and selectivity of the process. Its

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is effective in facilitating the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals and fine chemicals. Additionally, it is employed in transition metal-catalyzed reactions, such as hydrogenation and carbon-carbon bond formation, to enhance the efficiency and selectivity of the process. Its unique structure and stereochemistry contribute to its ability to control the spatial arrangement of atoms in the final product, ensuring high purity and desired optical activity.

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