1,3-Bis(2,6-diipropylphenyl)-4,5-dihydroimidazolium tetrafluoroborate

97%

Reagent Code: #143296
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Alias 1,3-bis(2,6-diisopropylphenyl)-4,5-dihydroimidazole tetrafluoroborate
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CAS Number 282109-83-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 478.42 g/mol
Formula C₂₇H₃₉BF₄N₂
badge Registry Numbers
MDL Number MFCD04971187
thermostat Physical Properties
Melting Point >300
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a precursor for generating N-heterocyclic carbenes (NHCs), this compound serves as an effective organocatalyst in various organic transformations. It is particularly valuable in transition-metal catalysis, where it stabilizes metal centers in cross-coupling reactions, olefin metathesis, and hydrogenation processes. Due to the steric bulk provided by the diisopropylphenyl groups, it enhances catalyst longevity and selectivity. Its tetrafluoroborate salt form improves stability and handling, making it suitable for use in air- and moisture-sensitive reactions when appropriate precautions are taken. Widely employed in academic and industrial research for developing new catalytic methodologies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿660.00
inventory 5g
10-20 days ฿3,220.00
inventory 25g
10-20 days ฿16,020.00
1,3-Bis(2,6-diipropylphenyl)-4,5-dihydroimidazolium tetrafluoroborate
Used as a precursor for generating N-heterocyclic carbenes (NHCs), this compound serves as an effective organocatalyst in various organic transformations. It is particularly valuable in transition-metal catalysis, where it stabilizes metal centers in cross-coupling reactions, olefin metathesis, and hydrogenation processes. Due to the steric bulk provided by the diisopropylphenyl groups, it enhances catalyst longevity and selectivity. Its tetrafluoroborate salt form improves stability and handling, making it suitable for use in air- and moisture-sensitive reactions when appropriate precautions are taken. Widely employed in academic and industrial research for developing new catalytic methodologies.
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