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

95%

Reagent Code: #237027
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CAS Number 850468-98-3

science Other reagents with same CAS 850468-98-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 434.4 g/mol
Formula C₁₈H₂₉F₆N₂OP
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral organocatalyst in asymmetric synthesis, particularly in enantioselective transformations such as aldol reactions, Michael additions, and epoxidations. Its imidazolium core with a defined stereochemistry enables efficient control over stereochemical outcomes, making it valuable in pharmaceutical and fine chemical manufacturing. The mesityl and fluorinated counterion groups enhance stability and solubility in organic solvents, supporting its use under a variety of reaction conditions. Often employed in low loadings due to high catalytic activity, it contributes to greener synthetic processes.

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inventory 100mg
10-20 days ฿7,010.00

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(S)-1-(1-Hydroxy-4-methylpentan-2-yl)-3-mesityl-4,5-dihydro-1H-imidazol-3-ium hexafluorophosphate(V)
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Used as a chiral organocatalyst in asymmetric synthesis, particularly in enantioselective transformations such as aldol reactions, Michael additions, and epoxidations. Its imidazolium core with a defined stereochemistry enables efficient control over stereochemical outcomes, making it valuable in pharmaceutical and fine chemical manufacturing. The mesityl and fluorinated counterion groups enhance stability and solubility in organic solvents, supporting its use under a variety of reaction conditions. Ofte

Used as a chiral organocatalyst in asymmetric synthesis, particularly in enantioselective transformations such as aldol reactions, Michael additions, and epoxidations. Its imidazolium core with a defined stereochemistry enables efficient control over stereochemical outcomes, making it valuable in pharmaceutical and fine chemical manufacturing. The mesityl and fluorinated counterion groups enhance stability and solubility in organic solvents, supporting its use under a variety of reaction conditions. Often employed in low loadings due to high catalytic activity, it contributes to greener synthetic processes.

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