(1S, 2S)-1,2-Bis(2-chlorophenyl)-1,2-ethanediamine dihydrochloride

95%

Reagent Code: #113030
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CAS Number 1052707-24-0

science Other reagents with same CAS 1052707-24-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 354.10 g/mol
Formula C₁₄H₁₆Cl₄N₂
badge Registry Numbers
MDL Number MFCD09836224
thermostat Physical Properties
Melting Point 230-235 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the field of organic synthesis and catalysis. It serves as a chiral ligand in asymmetric synthesis, facilitating the production of enantiomerically pure compounds, which are crucial in the development of pharmaceuticals. Its application is particularly significant in the synthesis of complex molecules where stereochemistry plays a critical role in biological activity. Additionally, it is employed in research settings to study and develop new catalytic processes that enhance the efficiency and selectivity of chemical reactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,748.00

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(1S, 2S)-1,2-Bis(2-chlorophenyl)-1,2-ethanediamine dihydrochloride
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This compound is primarily utilized in the field of organic synthesis and catalysis. It serves as a chiral ligand in asymmetric synthesis, facilitating the production of enantiomerically pure compounds, which are crucial in the development of pharmaceuticals. Its application is particularly significant in the synthesis of complex molecules where stereochemistry plays a critical role in biological activity. Additionally, it is employed in research settings to study and develop new catalytic processes that

This compound is primarily utilized in the field of organic synthesis and catalysis. It serves as a chiral ligand in asymmetric synthesis, facilitating the production of enantiomerically pure compounds, which are crucial in the development of pharmaceuticals. Its application is particularly significant in the synthesis of complex molecules where stereochemistry plays a critical role in biological activity. Additionally, it is employed in research settings to study and develop new catalytic processes that enhance the efficiency and selectivity of chemical reactions.

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