(1R,2R)-(–)-1,2-Bis[(2-pyridinylcarbonyl)amino]cyclohexane

97%

Reagent Code: #68248
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CAS Number 218290-24-5

science Other reagents with same CAS 218290-24-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 324.38 g/mol
Formula C₁₈H₂₀N₄O₂
badge Registry Numbers
MDL Number MFCD02684543
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its structure allows it to effectively coordinate with metals, enabling the induction of chirality in products. This makes it valuable in the synthesis of enantiomerically pure compounds, which are crucial in pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it is employed in research and development for exploring new catalytic processes and optimizing stereoselective transformations. Its application extends to academic studies focused on understanding chiral induction mechanisms and improving catalytic efficiency in organic synthesis.

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Test Parameter Specification
Appearance White to tan solid, powder, crystals

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿2,500.00
inventory 1g
10-20 days ฿3,370.00

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(1R,2R)-(–)-1,2-Bis[(2-pyridinylcarbonyl)amino]cyclohexane
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its structure allows it to effectively coordinate with metals, enabling the induction of chirality in products. This makes it valuable in the synthesis of enantiomerically pure compounds, which are crucial in pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it is employed in research and development for exploring new catalytic processes and optimizing ster

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its structure allows it to effectively coordinate with metals, enabling the induction of chirality in products. This makes it valuable in the synthesis of enantiomerically pure compounds, which are crucial in pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it is employed in research and development for exploring new catalytic processes and optimizing stereoselective transformations. Its application extends to academic studies focused on understanding chiral induction mechanisms and improving catalytic efficiency in organic synthesis.

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