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1,3-Bis(2,6-diisopropylphenyl)-4,5-dihydroimidazolium tetrafluoroborate / 100 KG

Purity: 95 %
Synonym: SIPr-HBF4; Bisdiisopropylphenyldihydroimidazoliumtetrafluoroborate; 1,3-Bis(2,6-di-i-propylphenyl)-4,5-dihydroimidazolium tetrafluoroborate; 1,3-Bis(2,6-diisopropylphenyl)-4,5-dihydro-1H-imidazol-3-ium tetrafluoroborate; N,N′-Bis(2,6-diisopropylphenyl)dihydroimidazolium tetrafluoroborate; 4,5-Dihydro-1,3-bis(2,6-diisopropylphenyl)imidazolium tetrafluoroborate
Molecular Formula: C27H39BF4N2
Molecular Weight: 478.42
SKU: MND-190080
CAS Number: 282109-83-5
MDL number: MFCD03412153
EC Number: 625-294-3
Form: solid
Packing size: 100 KG  



Safety Information


Hazard Statements

H314
H332

Precautionary Statements

P280
P303 + P361 + P353
P264
P501
P305 + P351 + P338
P261
P271
P304 + P340 + P310
P405
P260
P301 + P330 + P331
P363
P304 + P340
P321
P317
P316

Pictograms



Properties

Signal WordDanger
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

https://doi.org/10.1016/B978-0-08-099406-2.00001-7