2-Ethyl-4-methylimidazole
CAS: 931-36-2
Ref. 3D-FE37940
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Información del producto
- 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
- Ver más sinónimos
- 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
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.
Propiedades químicas
Consulta técnica sobre: 3D-FE37940 2-Ethyl-4-methylimidazole
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