1,3-Bis(2,6-diisopropylphenyl)-4,5-dihydroimidazolium tetrafluoroborate / 1 G
Safety Information
Hazard Statements
Precautionary Statements
Pictograms


Properties
Signal Word | Danger |
Flash Point (C) | Not available |
Flash Point (F) | Not available |
Melting Point | >300 |
Product Description
1,3-Bis(2,6-diisopropylphenyl)-4,5-dihydroimidazolium tetrafluoroborate is a specialized ionic liquid used in various advanced chemical reactions and processes. It stands out for its high thermal stability and excellent catalytic activity, making it ideal for applications in organic synthesis, particularly in the formation of complex molecules. This compound's unique structure allows it to act as an effective catalyst in reactions that involve difficult-to-handle substrates, enabling researchers and chemists to achieve higher yields and selectivities in their syntheses. Its broad applicability extends beyond academia to industrial settings, where it can facilitate the production of fine chemicals and pharmaceutical intermediates.
Application
In the field of chemistry, 1,3-Bis(2,6-diisopropylphenyl)-4,5-dihydroimidazolium tetrafluoroborate is utilized as a catalyst in organic synthesis, particularly in reactions that benefit from its thermal stability and nucleophilicity. Its use spans research laboratories to industrial-scale operations, aiding in the creation of pharmaceuticals, agrochemicals, and other specialty chemicals. This compound's ability to promote reactions efficiently at room temperature makes it a valuable tool in green chemistry initiatives, emphasizing sustainability and reduced environmental impact.
Articles:
- Retention or Inversion in Stereospecific Nickel-Catalyzed Cross-Coupling of Benzylic Carbamates with Arylboronic Esters: Control of Absolute Stereochemistry with an Achiral Catalyst
Publication Date: February 18, 2013
Michael R. Harris, Luke E. Hanna, Margaret A. Greene, Curtis E. Moore and Elizabeth R. Jarvo
https://doi.org/10.1021/ja311783k
- Selective Estrogen Receptor Modulators with Conformationally Restricted Side Chains. Synthesis and Structure−Activity Relationship of ERα-Selective Tetrahydroisoquinoline Ligands
Publication Date: December 22, 2004
Johanne Renaud, Serge François Bischoff, Thomas Buhl, Philipp Floersheim, Brigitte Fournier, Martin Geiser, Christine Halleux, Joerg Kallen, Hansjoerg Keller and Paul Ramage
https://doi.org/10.1021/jm040858p
- Chapter 1 - Progress in Quinoxaline Synthesis (Part 2)
Publication Date: Available online 6 September 2013
Vakhid A. Mamedov, Nataliya A. Zhukova