The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . 250285-32-6, formula is C27H37ClN2, Name is 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride. In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with an increase of the alkyl chain length of the alcohols. Safety of 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride.
Deng, Hao;Dong, Yujie;Shangguan, Yu;Yang, Fazhou;Han, Sheng;Wu, Jiaqi;Liang, Bo;Guo, Hongchao;Zhang, Cheng research published 《 Copper-Catalyzed Three-Component Carboboronation of Allenes Using Highly Strained Cyclic Ketimines as Electrophiles》, the research content is summarized as follows. A diastereoselective copper and NHC-ligand-catalyzed three-component difunctionalization of allenes RCH:C:CH2 with bis(pinacolato)diboron and 2H-azirines Ar1CHC(N)CAr2 to afford borylated allylaziridines Ar1CHC(NH)CAr2CHRC(Bpin):CH2 is described. The reaction exhibits complete diastereoselectivity and good yields, and the further chlorination of the corresponding borylated products was also performed. It is believed that the high ring-strain force of 2H-azirines facilitates the reaction. More chem. transformations of borylated allylaziridines are also reported.
250285-32-6, 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride, also known as 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride, is a useful research compound. Its molecular formula is C27H37ClN2 and its molecular weight is 425 g/mol. The purity is usually 95%.
1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride has been used to generate N-heterocyclic carbene catalysts for use in carbonylative cross-coupling of pyridyl halides with aryl boronic acids.
1,3-Bis(2,6-diisopropylphenyl)imidazolium Chloride is an imidazolium salt that is active against all stages of Trypanosoma cruzi and may represent a promising candidate for treatment of Chagas disease.
1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride is an organic compound that is used as a solvent. It was originally synthesized by reacting triethyl orthoformate with 2,6-diisopropylaniline. This reaction formed the corresponding imidazolium salt. The synthesis of this compound was later improved by using ring-opening polymerization of glycolide and furfural. 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride is mainly used to extract estradiol from urine samples in clinical laboratories., Safety of 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem