(1R,2R)-Bis(4-methoxyphenyl)-1,2-ethanediamine

98%

Reagent Code: #68243
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CAS Number 58520-03-9

science Other reagents with same CAS 58520-03-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272 g/mol
Formula C₁₆H₂₀N₂O₂
badge Registry Numbers
MDL Number MFCD08460192
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description Product Description

This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal catalysts. It is highly effective in facilitating enantioselective reactions, which are crucial for producing pharmaceuticals with high optical purity. The compound's chiral structure allows it to induce asymmetry in chemical reactions, making it valuable in the synthesis of complex organic molecules. Additionally, it is employed in research and development for designing new catalytic systems and exploring novel synthetic pathways in organic chemistry. Its application extends to the production of fine chemicals and intermediates used in the manufacture of drugs, agrochemicals, and specialty materials.

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Test Parameter Specification
Appearance White solid

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿17,880.00
inventory 1g
10-20 days ฿4,980.00

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(1R,2R)-Bis(4-methoxyphenyl)-1,2-ethanediamine
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This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal catalysts. It is highly effective in facilitating enantioselective reactions, which are crucial for producing pharmaceuticals with high optical purity. The compound's chiral structure allows it to induce asymmetry in chemical reactions, making it valuable in the synthesis of complex organic molecules. Additionally, it is employed in research and development for

This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal catalysts. It is highly effective in facilitating enantioselective reactions, which are crucial for producing pharmaceuticals with high optical purity. The compound's chiral structure allows it to induce asymmetry in chemical reactions, making it valuable in the synthesis of complex organic molecules. Additionally, it is employed in research and development for designing new catalytic systems and exploring novel synthetic pathways in organic chemistry. Its application extends to the production of fine chemicals and intermediates used in the manufacture of drugs, agrochemicals, and specialty materials.

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