CAS 3034-38-6
:5-Nitroimidazolo
- 1H-4-Nitroimidazole
- 1H-5-Nitroimidazole
- 1H-Imidazole, 4-nitro-
- 1H-Imidazole, 5-nitro-
- 4(5)-Nitroimidazole
- 4-Nitro-1H-imidazole
- 5-Nitro-1H-imidazole
- 5-Nitroimidazole
- Imidazole, 4(or 5)-nitro-
- Imidazole, 4-nitro-
- NSC 50359
- Vedi altri sinonimi
4-Nitroimidazole
CAS:Formula:C3H3N3O2Purezza:>98.0%(GC)Colore e forma:White to Light yellow powder to crystalPeso molecolare:113.084-Nitroimidazole, 97%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formula:C3H3N3O2Purezza:97%Colore e forma:Powder, White to pale cream to pale yellowPeso molecolare:113.084-Nitro-1H-imidazole
CAS:4-Nitro-1H-imidazoleFormula:C3H3N3O2Purezza:98%Colore e forma: off-white powderPeso molecolare:113.07481g/molMetronidazole EP Impurity B (4-Nitroimidazole)
CAS:Formula:C3H3N3O2Colore e forma:White To Off-White SolidPeso molecolare:113.084-Nitroimidazole
CAS:Formula:C3H3N3O2Purezza:≥ 97%Colore e forma:White to off-white or yellow powderPeso molecolare:113.08GB/T 21318-2007, SN/T 1928-2007 10 Nitroimidazoles 100 µg/mL in Methanol
CAS:Prodotto controllatoColore e forma:MixtureRef: ST-EA-CP-M18002
10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiesta4-Nitro-1H-imidazole
CAS:Prodotto controllatoApplications Metronidazole (M338880) derivative, an antibacterial in the treatment of rosacea and inflammatory bowel disease.
References Khan, K. et al.; Am. J. Gastroenterol. 106, 661 (2011)Formula:C3H3N3O2Colore e forma:NeatPeso molecolare:113.074-Nitroimidazole
CAS:4-Nitroimidazole has a redox potential that is well suited to the reduction of nitro groups. It is an antimicrobial agent that inhibits the growth of microorganisms by inhibiting DNA synthesis. 4-Nitroimidazole can be used for the treatment of infectious diseases such as tuberculosis, leprosy, and brucellosis. In rat liver microsomes, 4-nitroimidazole reacts with NADPH to produce a nitro group and an imidazole ring with a new configuration. The reaction mechanism is based on electron transfer from NADPH to the nitro group in 4-nitroimidazole via a series of reactions that involve cytochrome P450 enzymes. This reaction has kinetic energy and matrix effects that affect its pharmacokinetics and pharmacodynamics.
Formula:C3H3N3O2Purezza:Min. 95%Colore e forma:White PowderPeso molecolare:113.07 g/mol













