67768-61-0

Basic information

• Product Name: 1-cyclohexyl-iMidazole
• Synonyms: 1-cyclohexyl-iMidazole;1-Cyclohexyl-1H-iMidazole;1H-Imidazole, 1-cyclohexyl-
• CAS NO: 67768-61-0
• Molecular Formula: C₉H₁₄N₂
• Molecular Weight: 150.22086
• Mol File: 67768-61-0.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 302.9±11.0 °C(Predicted)
• Appearance: /
• Density: 1.10±0.1 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 7.21±0.10(Predicted)
• CAS DataBase Reference: 1-cyclohexyl-iMidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-cyclohexyl-iMidazole(67768-61-0)
• EPA Substance Registry System: 1-cyclohexyl-iMidazole(67768-61-0)

Safety Data

• Hazardous Substances Data: 67768-61-0(Hazardous Substances Data)

Usage

General Description

1-cyclohexyl-iMidazole is an organic compound with the chemical formula C9H14N2. It is a heterocyclic compound with a cyclohexane ring and an imidazole ring, and it is commonly used as a reagent in organic synthesis. 1-cyclohexyl-iMidazole is known to have anti-fungal properties, making it useful in pharmaceutical applications, particularly in the development of antifungal drugs. It is also used as a corrosion inhibitor and an intermediate in the production of various chemicals. Additionally, 1-cyclohexyl-iMidazole has been studied for its potential anti-cancer properties, as well as its ability to inhibit the growth of certain bacteria. However, it is important to handle this compound with care, as it can be harmful if ingested or 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

• 1240324-94-0 C₁₄H₂₄N₂O 
• 1240324-91-7 3-(1-cyclohexyl-1H-imidazol-2-yl)pentan-3-ol 
• 1240324-92-8 1-(1-cyclohexyl-1H-imidazol-2-yl)-1-phenylethanol 
• 1240324-93-9 1-(1-cyclohexyl-1H-imidazol-2-yl)-2,2-dimethylpropan-1-ol 
• 1008140-51-9 Br^(1-)*C₁₅H₂₀N₃⁽¹⁺⁾ 
• 922192-61-8 1-(cyclohexyl)-3-ferrocenylethylimidazolium iodide 

Relevant articles and documents

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-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

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.