(S)-1-(1-Hydroxy-3-phenylpropan-2-yl)-3-mesityl-4,5-dihydro-1H-imidazol-3-ium hexafluorophosphate(V)

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Reagent Code: #69001
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CAS Number 882992-52-1

science Other reagents with same CAS 882992-52-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 468.42 g/mol
Formula C₂₁H₂₇F₆N₂OP
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 enantioselective reactions. It serves as a chiral catalyst or ligand in organic transformations, enabling the production of enantiomerically pure compounds, which are crucial in pharmaceuticals and fine chemicals. Its structure, featuring a mesityl group and imidazolium core, enhances stability and reactivity in catalytic processes. Additionally, it is employed in the development of advanced materials and in research focused on stereochemistry and chiral induction.

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inventory 50mg
10-20 days ฿7,092.00

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(S)-1-(1-Hydroxy-3-phenylpropan-2-yl)-3-mesityl-4,5-dihydro-1H-imidazol-3-ium hexafluorophosphate(V)
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This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. It serves as a chiral catalyst or ligand in organic transformations, enabling the production of enantiomerically pure compounds, which are crucial in pharmaceuticals and fine chemicals. Its structure, featuring a mesityl group and imidazolium core, enhances stability and reactivity in catalytic processes. Additionally, it is employed in the development of advanced materials and in resear

This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. It serves as a chiral catalyst or ligand in organic transformations, enabling the production of enantiomerically pure compounds, which are crucial in pharmaceuticals and fine chemicals. Its structure, featuring a mesityl group and imidazolium core, enhances stability and reactivity in catalytic processes. Additionally, it is employed in the development of advanced materials and in research focused on stereochemistry and chiral induction.

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