25372-09-2

Usage

Uses

Used in Pharmaceutical Industry:
1-(2,6-dimethylphenyl)-1H-imidazole is used as an antifungal agent for its ability to inhibit the growth of certain fungi, making it a valuable component in the development of medications targeting fungal infections.
Used in Coordination Chemistry Research:
In the field of research and development, 1-(2,6-dimethylphenyl)-1H-imidazole is used as a ligand for its capacity to form coordination complexes with transition metals, contributing to the advancement of coordination chemistry.
Used in Industrial Applications:
1-(2,6-dimethylphenyl)-1H-imidazole has also been studied for its potential use as a corrosion inhibitor, which could be beneficial in protecting materials from the damaging effects of corrosion in various industrial settings.
The provided materials highlight the versatility of 1-(2,6-dimethylphenyl)-1H-imidazole in different sectors, showcasing its potential as an active pharmaceutical agent, a research tool in coordination chemistry, and a protective agent in industrial applications.

Upstream product

• 288-32-4 1H-imidazole 
• 576-22-7 2-Bromo-m-xylene 
• 12775-96-1 copper 
• 50-00-0 formaldehyd 
• 131543-46-9 Glyoxal 
• 87-62-7 2,6-dimethylaniline 
• 576-26-1 2.6-dimethylphenol 
• 530-62-1 1,1'-carbonyldiimidazole 

Downstream Products

• 1016260-29-9 3-(2,6-dimethylphenyl)-1-[(2-diphenylphosphinoferrocenyl)ethyl]-3H-imidazolium iodide 
• 1355955-84-8 1-(2,6-dimethylphenyl)-3-[((4bS,8R,8aR)-2-isopropyl-8-(methoxycarbonyl)-4b,8-dimethyl-4b,5,6,7,8,8a,9,10-octahydrophenanthren-3-yl)methyl]-3H-imidazol-1-ium chloride 
• 1385782-69-3 3-[3,28-diacetoxylup-20⁽²⁹⁾-en-30-yl]-1-(2,6-dimethylphenyl)-1H-imidazol-3-ium bromide 
• 1448545-87-6 C₂₃H₂₅FeN₂⁽¹⁺⁾*Cl^(1-) 

Relevant academic research and scientific papers

High-yield synthesis of novel imidazoles and triazoles from alcohols and phenols

A variety of alcohols and phenols are converted into their corresponding imidazoles and triazoles in high yields by a facile reaction with N,N1-carbonyldiimidazole (CDI) or N,N1-carbonylditriazole (CDT) in acetonitrile. The reactions of allylic alcohols, enols and phenols with CDI or CDT are unprecedented. Evidence is provided which suggests that the reaction with alcohols proceeds via the corresponding carbamates by an S(N)i mechanism.

Synthesis and characterization of Ag(I) complexes derived from new N-heterocyclic carbenes

Two new unsymmetrical imidazolium salts viz., [1-(4-ethylphenyl)-3-propyl-1H-imidazole-3-ium bromide] (3) and [1-(2,6-dimethylphenyl)-3-propyl-1H-imidazole-3-ium bromide] (4) have been synthesized via the reaction of propyl bromide with imidazole derivati

One pot tandem dual CC and CO bond reductions in the β-alkylation of secondary alcohols with primary alcohols by ruthenium complexes of amido and picolyl functionalized N-heterocyclic carbenes

Two different classes of ruthenium complexes, namely, [1-mesityl-3-(2,6-Me2-phenylacetamido)-imidazol-2-ylidene]Ru(p-cymene)Cl (1c) and {[1-(pyridin-2-ylmethyl)-3-(2,6-Me2-phenyl)-imidazol-2-ylidene]Ru(p-cymene)Cl}Cl (2c), successfully catalyzed the one-pot tandem alcohol-alcohol coupling reactions of a variety of secondary and primary alcohols, in moderate to good yields of ca. 63-89%. The mechanistic investigation performed on two representative catalytic substrates, 1-phenylethanol and benzyl alcohol using the neutral ruthenium (1c) complex showed that the catalysis proceeded via a partially reduced CC hydrogenated carbonyl species, [PhCOCH2CH2Ph] (3′), to the fully reduced CO and CC hydrogenated secondary alcohol, [PhCH(OH)CH2CH2Ph] (3). Furthermore, the time dependent study showed that the major product of the catalysis modulated between (3′) and (3) during the catalysis run performed over an extended period of 120 hours. Finally, the practical utility of the alcohol-alcohol coupling reaction was demonstrated by preparing five different flavan derivatives (13-17) related to various bioactive flavonoid natural products, in a one-pot tandem fashion.

Suzuki-Miyaura coupling with high turnover number using an N-acyl-N-heterocyclic carbene palladacycle precursor

A simple N-acylimidazolium salt precursor to a NHC-complexed palladacyclic ligand gives high turnover numbers (107) for Suzuki-Miyaura coupling and is applied to the preparation of biaryls used in the synthesis of coumarins. The results suggest that N-acyl-NHC derivatives can contribute to further expanding the rich chemistry of NHCs.

Ion channel modulating agents

The present invention relates to ion channel modulating agents. More particularly, the present invention relates to a particular class of chemical compounds represented by general Formula (I) and a pharmaceutically acceptable salt or an oxide or a hydrate