| Availability: | |
|---|---|
| CAS Non. | 3034-50-2 |
| Synonyma | 4-Formylimidazole 1H-Imidazole-4-carbaldehyde 1H-imidazole-5-carbaldehyde 1-(1H-imidazol-5-yl)ethanone 4(5) -Formylimidazole 4(5)-imidazolecarboxaldehyde 4-Aldehyde Imidazole 4(5)-Imidazole Aldehyde |
| EINECS No. | 221-227-3 |
| Formulae hypotheticae | C₄H₄N₂O |
| Pondus hypotheticum (g / mol) | 96.09 |
| Densitas (g/cm3) | 1.19 |
| Aspectus | Flavo flavo ad crystallinum pulveris |
| Puritas (%) | 99min (HPLC) |
| Aqua Content | ≤ 0.5%(KF) |
| Exustio Point(℃) | 172-176 |
| Solubilitas | Solutum in aqua calida, DMSO et methanolo |
Imidazole-4-carboxaldehyde versatile chemicum compositum est cum CAS numero 3034-50-2. This product is an important derivative of imidazole, featuring a formyl group in the 4-position of the imidazole ring. Imidazole-4-carboxaldehyde medium est pretiosum in investigationibus chemicis et pharmaceuticis ob singularem structuram et coetus functionis suae, idoneus faciens pro amplis applicationibus.
Applicationem
1.Pharmaceutical Synthesis
Imidazole-4-carboxaldehyde adhibetur pro praecursor in praeparatione C17, 20-lyase inhibitores, quae significant ad curationem cancri prostatae androgeni-dependens. Usurpatur etiam in synthesi aliarum compositionum biologicarum activarum, etiam medicamentorum antimalarialium.
2.Chemosensor Fabricatio
Hoc compositum adiuvatur in chemosensoribus colorimetric evolutionis, quae necessariae sunt ad deprehendendas species specificas chemicas.
3.Dye Synthesis
In synthesi novorum donatoris-π-acceptoris (D-π-A) speciei colores implicatur, quae potentiales applicationes in scientiis materialibus et electronicis organicis habent.
4.Metal Complexes
Imidazole-4-carboxaldehyde complexorum chiralorum nickel(II) synthesizare adhibetur, ut Ni(II)H3L(ClO4)2, quae applicationes in catalysi et materiarum scientia habent.
Sarcina
25kg/orum
Repono
Sub nitrogenium / argonis ad 2-8°C thesaurum diuturnum firmitatis.