2-Ethyl-4-methylimidazole

CAS: 931-36-2

Ref. 3D-FE37940

Produktinformation

• Name: 2-Ethyl-4-methylimidazole
• Synonyme: 1H-Imidazole, 2-ethyl-4-methyl-, 1H-Imidazole, 2-ethyl-5-methyl-, 2-Ethyl-4-methyl imidazole, 2-Ethyl-4-methyl-1H-imidazole, 2-Ethyl-4-methyl-3H-imidazole, 2-Ethyl-4-methylimidazol, 2-Etil-4-Metilimidazol, 2-ethyl-5-methyl-1H-imidazole, 2E4Mz, 4-Methyl-2-ethyl-1H-imidazole, 4-methyl-2-Ethylimidazole, B 2, B 2 (curing catalyst), Curazol 2E4MZ, Curezol 2E4MZ2, Curezol-2E4MZ, Dyhard MI-C, E 0232, Emi 24, Emi-70, Emi24, Epicure-EMI-24, Imicure-EMI-24, Imidazole (1H), 2-Ethyl-4-Methyl-, Imidazole, 2-ethyl-4(or 5)-methyl-, Imidazole, 2-ethyl-4-methyl-, JER Cure EMI 24, Labotest-Bb Ltbb000689, Nsc 82315, Omicure 24EMI, Texnol EM 24, Timtec-Bb Sbb004334
• CAS: 931-36-2

Beschreibung

2-Ethyl-4-methylimidazole is an aromatic hydrocarbon that is used in the synthesis of a boron nitride template molecule. It is also used as a precursor for the synthesis of magnetic resonance contrast agents, which are used for MRI. The chemical structure of 2-ethyl-4-methylimidazole has been determined using magnetic resonance spectroscopy to be a crosslink between an aromatic ring and a methyl group. It reacts with hydrochloric acid to produce chloride, which can be detected using magnetic resonance spectroscopy at a detection sensitivity of 0.1 ppm. 2-Ethyl-4-methylimidazole has also been shown to have thermal activation energies (E) of 14.3 kcal/mol and 12.3 kcal/mol at 20 °C and 100 °C respectively, making it suitable for use in reactions that require high temperatures such as reactions with sodium carbonate or zirconium oxide.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 110.16 g/mol
• Formel: C₆H₁₀N₂
• Reinheit: Min. 95%
• InChl: InChI=1S/C6H10N2/c1-3-6-7-4-5(2)8-6/h4H,3H2,1-2H3,(H,7,8)
• InChI Key: InChIKey=ULKLGIFJWFIQFF-UHFFFAOYSA-N
• SMILES: CCc1ncc(C)[nH]1