89128-07-4 Usage
Nitroimidazole derivative
A compound containing a nitro group and an imidazole ring This refers to the specific functional groups present in the structure, which give the compound its unique properties and reactivity.
Building block in organic synthesis
Used in the production of pharmaceuticals and agrochemicals This highlights the compound's role as an intermediate in the synthesis of various target molecules, particularly in the fields of medicine and agriculture.
Potential anti-parasitic and anti-microbial agent
Inhibits certain enzymes and biological processes in microorganisms This refers to the compound's ability to interfere with the normal functioning of parasites and microorganisms, making it a potential candidate for treating infections.
Corrosion inhibitor
Investigated for its potential application in protecting metal surfaces This indicates that the compound may have properties that can prevent or减缓 the corrosion of metals, which is important for maintaining the integrity and longevity of metal structures.
Versatile chemical
Various industrial and research applications This emphasizes the wide range of potential uses for 1-ETHYL-2-METHYL-4-NITRO-1H-IMIDAZOLE, making it a valuable compound in both industry and scientific research.
Check Digit Verification of cas no
The CAS Registry Mumber 89128-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,2 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89128-07:
(7*8)+(6*9)+(5*1)+(4*2)+(3*8)+(2*0)+(1*7)=154
154 % 10 = 4
So 89128-07-4 is a valid CAS Registry Number.
89128-07-4Relevant articles and documents
Transition-metal-catalyzed arylation of nitroimidazoles and further transformations of manipulable nitro group
Iaroshenko, Viktor O.,Gevorgyan, Ashot,Mkrtchyan, Satenik,Arakelyan, Knar,Grigoryan, Tatevik,Yedoyan, Julietta,Villinger, Alexander,Langer, Peter
, p. 2103 - 2119 (2015/04/14)
Pd- or Ni-catalyzed C-H arylation of 4-nitroimidazole derivatives directed by a manipulable nitro group was developed. The reaction tolerates a wide range of substituted aryl halides and 4-nitroimidazoles. The experiments indicated that the nitro group has influence on regioselectivity of the reaction. In addition, we have shown that the efficiency of the Suzuki-Miyaura cross-coupling reaction of nitroimidazoles is slightly lower in comparison to the direct C-H arylation. The exploration of the chemical potential of the nitro group and a putative reaction mechanism are discussed.
Solid-liquid phase-transfer catalytic method for N-alkylation of nitroimidazole
Liu,Chen,Cao,Li
, p. 2611 - 2615 (2007/10/02)
A variety of 1-alkyl-2-methyl-4-nitroimidazoles have been synthesized with a solid-liquid phase-transfer catalytic method in excellent yields.
