1-(2,4,6-Trimethylphenyl)-3-[(1R,2R,3R,5S)-(-)-isopinocampheyl]imidazolium chloride

≥95%

Reagent Code: #70574
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CAS Number 1583244-12-5

science Other reagents with same CAS 1583244-12-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 358.95 g/mol
Formula C₂₂H₃₁ClN₂
badge Registry Numbers
MDL Number MFCD28144534
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description Product Description

This compound is primarily utilized as a chiral ionic liquid or catalyst in asymmetric synthesis, particularly in organic transformations where enantioselectivity is crucial. Its unique structure, combining an imidazolium core with a chiral isopinocampheyl group, makes it effective in facilitating stereocontrolled reactions such as hydrogenation, cyclopropanation, and Diels-Alder reactions. It is also employed in the development of chiral materials and as a phase-transfer catalyst in biphasic systems, enhancing reaction efficiency and selectivity. Additionally, its application extends to the field of green chemistry, where it serves as a reusable and environmentally friendly alternative to traditional catalysts.

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inventory 100mg
10-20 days ฿8,829.00

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1-(2,4,6-Trimethylphenyl)-3-[(1R,2R,3R,5S)-(-)-isopinocampheyl]imidazolium chloride
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This compound is primarily utilized as a chiral ionic liquid or catalyst in asymmetric synthesis, particularly in organic transformations where enantioselectivity is crucial. Its unique structure, combining an imidazolium core with a chiral isopinocampheyl group, makes it effective in facilitating stereocontrolled reactions such as hydrogenation, cyclopropanation, and Diels-Alder reactions. It is also employed in the development of chiral materials and as a phase-transfer catalyst in biphasic systems, en

This compound is primarily utilized as a chiral ionic liquid or catalyst in asymmetric synthesis, particularly in organic transformations where enantioselectivity is crucial. Its unique structure, combining an imidazolium core with a chiral isopinocampheyl group, makes it effective in facilitating stereocontrolled reactions such as hydrogenation, cyclopropanation, and Diels-Alder reactions. It is also employed in the development of chiral materials and as a phase-transfer catalyst in biphasic systems, enhancing reaction efficiency and selectivity. Additionally, its application extends to the field of green chemistry, where it serves as a reusable and environmentally friendly alternative to traditional catalysts.

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