37572-50-2

Basic information

• Product Name: 1,1'-DIETHYL-1H,1'H-[2,2']BIIMIDAZOLYL
• Synonyms: 1,1'-DIETHYL-1H,1'H-[2,2']BIIMIDAZOLYL;1-ethyl-2-(1-ethylimidazol-2-yl)imidazole
• CAS NO: 37572-50-2
• Molecular Formula: C10H14N4
• Molecular Weight: 190.24496
• Mol File: 37572-50-2.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,1'-DIETHYL-1H,1'H-[2,2']BIIMIDAZOLYL(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1'-DIETHYL-1H,1'H-[2,2']BIIMIDAZOLYL(37572-50-2)
• EPA Substance Registry System: 1,1'-DIETHYL-1H,1'H-[2,2']BIIMIDAZOLYL(37572-50-2)

Safety Data

• Hazardous Substances Data: 37572-50-2(Hazardous Substances Data)

Usage

General Description

1,1'-DIETHYL-1H,1'H-[2,2']BIIMIDAZOLYL is a chemical compound that belongs to the imidazole family. It is a symmetrically substituted derivative of imidazole, with two ethyl groups attached to the nitrogen atoms at positions 1 and 1'. 1,1'-DIETHYL-1H,1'H-[2,2']BIIMIDAZOLYL is primarily used in the pharmaceutical and agrochemical industries as a building block for the synthesis of various drugs and pesticides. It also has potential applications in research and development due to its unique structure and properties. The compound is known for its ability to form coordination complexes with metal ions, making it useful in catalysis and material science. Overall, 1,1'-DIETHYL-1H,1'H-[2,2']BIIMIDAZOLYL is a versatile chemical with diverse applications across different fields.

Upstream product

• 75143-01-0 1,1'-divinyl-1H,1'H-2,2'-biimidazole 
• 492-98-8 2,2'-biimidazole 
• 7098-07-9 N-Ethylimidazole 
• 75-03-6 ethyl iodide 

Relevant articles and documents

SYNTHESIS AND SPECTRAL STUDIES OF VINYL DERIVATIVES OF 2,2'-DIIMIDAZOLYL

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Metallophilic interactions in stacked dinuclear rhodium 2,2′-biimidazole carbonyl complexes

Non-covalent metallophilic interactions were studied by investigating the stacking of two neutral rhodium complexes [Rh2I(R 2bim)Cl2(CO)4] (R = Et, ethyl or Pr, propyl) in the solid state. Both dinuclear complexes formed infinite arrays of square planar d8 rhodium centres with intramolecular Rh...Rh distances of 3.1781(5) A (R = Et) and 3.1469(3) A (R = Pr) and the intermolecular Rh...Rh distances of 3.4345(6) A (R = Et) and 3.4403(3) A (R = Pr) between the adjacent molecules. The crystalline solids were stable and did not contain any solvent of crystallization. The effect of the metallophilic interactions on the absorption properties were studied using TD-DFT methods. The computational results indicate a red shift with a shortening Rh...Rh distance. Experimentally, bathochromic effects were also observed. The colour of the crystals was found to be dependent on the temperature, shape of the crystal, and the direction of the incoming light. The general appearance of the crystal was strongly affected by the linearly arranged metal atoms. Both crystalline materials had a metallic lustre typical of chain-like metal systems with metal-metal interactions. The Royal Society of Chemistry.