67768-61-0

Usage

Uses

Used in Pharmaceutical Applications:
1-cyclohexyl-iMidazole is used as an active pharmaceutical ingredient for its anti-fungal properties, targeting the development of antifungal drugs to combat fungal infections.
Used in Organic Synthesis:
As a reagent, 1-cyclohexyl-iMidazole is used in various organic synthesis processes, facilitating the creation of a range of chemical compounds.
Used in Corrosion Inhibition:
1-cyclohexyl-iMidazole is used as a corrosion inhibitor, helping to protect materials from degradation due to environmental factors.
Used in Chemical Production:
1-cyclohexyl-iMidazole serves as an intermediate in the production of various chemicals, contributing to the synthesis of a multitude of compounds.
Used in Anticancer Research:
1-cyclohexyl-iMidazole is used as a subject of research for its potential anti-cancer properties, with studies exploring its effects on inhibiting the growth of cancer cells.
Used in Bacterial Growth Inhibition:
It is also used in research to study its ability to inhibit the growth of certain bacteria, which could lead to new antimicrobial agents.
It is crucial to handle 1-cyclohexyl-iMidazole with care due to its potential harmful effects if ingested or if it comes into contact with the skin or eyes.

Upstream product

• 50-00-0 formaldehyd 
• 131543-46-9 Glyoxal 
• 108-91-8 cyclohexylamine 
• 288-32-4 1H-imidazole 

Downstream Products

• 496067-62-0 1-(((S)-4',5'-dihydro-2'-(1-adamantyl)-4'-oxazolyl)ethyl)-3-cyclohexylimidazolium iodide 
• 937790-30-2 3-cyclohexyl-1-(3,5-di-tert-butyl-2-hydroxy-phenyl)-3H-imidazol-1-ium; bromide 
• 866599-61-3 (1R,2R)-1,2-bis(1-cyclohexylimidazol-2-thio-3-methyl)cyclopentane 
• 866599-60-2 (1S,2S)-1,2-bis(1-cyclohexylimidazol-2-thio-3-methyl)cyclopentane 
• 849239-92-5 2,4,5-tribromo-1-cyclohexyl-1H-imidazole 
• 922192-61-8 1-(cyclohexyl)-3-ferrocenylethylimidazolium iodide 
• 1008140-51-9 Br^(1-)*C₁₅H₂₀N₃⁽¹⁺⁾ 
• 1240324-93-9 1-(1-cyclohexyl-1H-imidazol-2-yl)-2,2-dimethylpropan-1-ol 
• 1240324-92-8 1-(1-cyclohexyl-1H-imidazol-2-yl)-1-phenylethanol 
• 1240324-91-7 3-(1-cyclohexyl-1H-imidazol-2-yl)pentan-3-ol 
• 1240324-94-0 C₁₄H₂₄N₂O 

Relevant academic research and scientific papers

Synthesis and structure of palladium(II) complexes supported by bis-NHC pincer ligands for the electrochemical activation of CO2

A series of bis-NHC pincer complexes of palladium(II) have been prepared and characterized. These pyridyl-spaced dicarbene complexes ([(PDCR)Pd(MeCN)](PF6)2) were synthesized with substituents of varying steric bulk at the

Isoprene as lithiation mediator: Synthesis of 2-substituted 1-alkylimidazole derivatives

The lithiation of different imidazoles bearing a primary (i.e., butyl, pentyl, dodecyl) or secondary (i.e., cyclohexyl, 1-methylheptyl) alkyl substituent on the nitrogen has been successfully achieved by means of an isoprene-mediated protocol. The subsequent reaction of the 2-lithioimidazole intermediates with different electrophiles leads to the formation of interesting 1,2-disubstituted imidazoles. Georg Thieme Verlag Stuttgart · New York.

Isoprene-mediated lithiation of 1-alkylimidazoles: Chiral induction of the alkyl substituent

The isoprene-mediated lithiation of imidazoles bearing a secondary alkyl substituent at the nitrogen (7, 8 and 13) and the subsequent nucleophilic addition to different electrophiles allows the preparation of the corresponding 2-functionalized imidazoles

Cycloalkyl heterocycles for treating Hepatitis C virus

Compounds of Formula I are disclosed which inhibit hepatitis C NS5B RNA-dependent RNA polymerase and are useful for treating hepatitis C. Compositions and methods of using these compounds are also disclosed.

Copper carbenoid mediated N-alkylation of imidazoles and its use in a novel synthesis of bifonazole

1H-Imidazoles are readily N-alkylated by a Cu(acac)2 mediated reaction with α-diazocarbonyl compounds or with diazoalkanes generated in situ from the corresponding p-toluensulfonyl hydrazones. The antifungal agent bifonazole was prepared by the latter method. Graphical Abstract.

Optically active iridium imidazol-2-ylidene-oxazoline complexes: Preparation and use in asymmetric hydrogenation of arylalkenes

This work explores the potential of iridium complexes of the N-heterocyclic carbene oxazoline ligands 1 in asymmetric hydrogenations of arylalkenes. The accessible carbene precursors, imidazolium salts 2, and robust iridium complexes 5 facilitated a disco

Synthesis of 1-alkylimidazoles

A mechanistic investigation of the synthesis of imidazole and 1- alkylimidazoles has led to an improved synthesis starting from glyoxal, formaldehyde and alkylammonium chlorides.

3-Imidazolium cephalosporin derivatives

A cephalosporin compound substituted by imidazolium ring in 3-position of cephem having the following formula (I), and pharmaceutically acceptable salt thereof, STR1 wherein R1 is an organic residue known in β-lactam antibiotics, R2 is hydrogen atom or methoxy, n is 0 or 1, A is a nitrogen-containing group constituting imidazolium ring, is useful as an agent for preventing and treating bacterial infections.