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1,3-Bis-(2,6-diisopropylphenyl)imidazolinium chloride / 100 KG

Purity: >95%
Synonym: N,N′-(2,6-Diisopropylphenyl)dihydroimidazolium chloride
Molecular Formula: C27H39ClN2
Molecular Weight: 427.06
SKU: MND-190081
CAS Number: 258278-25-0
MDL number: MFCD07369796
EC Number: 627-991-8
PubChem: 2734918
Form: solid
Packing size: 100 KG  



Safety Information


Hazard Statements

H315
H319
H335

Precautionary Statements

P280
P264
P501
P305 + P351 + P338
P261
P271
P405
P302 + P352
P362 + P364
P403 + P233
P304 + P340
P321
P264 + P265
P319
P332 + P317
P337 + P317

Pictograms



Properties

Signal WordWarning

 Product Description

1,3-Bis-(2,6-diisopropylphenyl)imidazolinium chloride is a potent organocatalyst designed for use in a variety of chemical reactions. It is recognized for its exceptional stability and strong acidity, which enable it to effectively catalyze reactions that are challenging to perform with traditional methods. This compound's unique structure allows it to interact favorably with a wide range of substrates, leading to enhanced reaction rates and improved product selectivity. Its utility is not limited to academic research; it also finds application in industrial settings, particularly in the production of fine chemicals and pharmaceuticals, where precise control over reaction outcomes is crucial.

 

Application

In the realm of chemistry, 1,3-Bis-(2,6-diisopropylphenyl)imidazolinium chloride serves as an organocatalyst, facilitating reactions that benefit from its acidic nature and structural features. Its use spans from laboratory-scale experiments to industrial processes, playing a significant role in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. This compound's ability to enhance reaction efficiency and product quality positions it as a valuable asset in the pursuit of sustainable and environmentally friendly chemical manufacturing processes.

 

 

Articles:

- Efficient synthetic protocols for the preparation of common N-heterocyclic carbene precursors

Publication Date: 25 Nov 2015

Morgan Hans,  Jan Lorkowski,  Albert Demonceau and  Lionel Delaude

https://doi.org/10.3762/bjoc.11.252

 

- Synthesis of bis-oxazoline-ruthenium(II)-arene complexes.: Combined catalytic isomerisation and Claisen rearrangement of bis-allyl ether

Publication Date: Available online 12 October 2002

Hamed Ben Ammar, Jérôme Le Nôtre, Mansour Salem, Mohamed T Kaddachi, Pierre H Dixneuf

https://doi.org/10.1016/S0022-328X(02)01881-8

 

- A Comparative Study on (NHC)Pd(acac)Cl Complexes (NHC = N-heterocyclic carbene): Indications for the Origin of the Different Reactivity of Saturated and Unsaturated NHC in Cross-Coupling Reactions

Publication Date: September 9, 2009

Ole H. Winkelmann, Andrei Riekstins, Steven P. Nolan and Oscar Navarro

https://doi.org/10.1021/om900677v