(1R,2R)-()-1,2-Bis(4-dimethylaminophenyl)ethylenediaminetetrahydrochloride

97%

Reagent Code: #68241
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CAS Number 866267-84-7

science Other reagents with same CAS 866267-84-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 298.43 g/mol
Formula C₁₈H₂₆N₄
badge Registry Numbers
MDL Number MFCD09839134
inventory_2 Storage & Handling
Storage 2-8°C, dry, inert gas

description Product Description

Used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is employed in the production of pharmaceuticals to create optically active compounds, enhancing the efficacy and reducing side effects of drugs. Additionally, it serves as a catalyst in organic transformations, such as hydrogenation and carbon-carbon bond formation, improving reaction efficiency and selectivity. Its role in stereochemistry makes it valuable in research and development of new therapeutic agents and fine chemicals.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,172.00

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(1R,2R)-()-1,2-Bis(4-dimethylaminophenyl)ethylenediaminetetrahydrochloride
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Used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is employed in the production of pharmaceuticals to create optically active compounds, enhancing the efficacy and reducing side effects of drugs. Additionally, it serves as a catalyst in organic transformations, such as hydrogenation and carbon-carbon bond formation, improving reaction efficiency and selectivity. Its role in stereochemistry makes it valuable in research and develop

Used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is employed in the production of pharmaceuticals to create optically active compounds, enhancing the efficacy and reducing side effects of drugs. Additionally, it serves as a catalyst in organic transformations, such as hydrogenation and carbon-carbon bond formation, improving reaction efficiency and selectivity. Its role in stereochemistry makes it valuable in research and development of new therapeutic agents and fine chemicals.

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