79456-89-6 Usage
Uses
Used in Pharmaceutical Industry:
Ethanone, 1-(4-bromophenyl)-2-(2-methyl-4-nitro-1H-imidazol-1-yl)is used as a potential pharmaceutical agent for its possible bioactivity due to the imidazole moiety. Ethanone, 1-(4-bromophenyl)-2-(2-methyl-4-nitro-1H-imidazol-1-yl)may be further investigated for its therapeutic effects in treating various diseases or conditions, pending the results of additional research.
Used in Agricultural Industry:
In agriculture, Ethanone, 1-(4-bromophenyl)-2-(2-methyl-4-nitro-1H-imidazol-1-yl)could be explored for its potential as a pesticide or herbicide, leveraging its chemical properties to control pests or weeds, provided that its safety and efficacy are confirmed through rigorous testing.
Used in Material Science:
Ethanone, 1-(4-bromophenyl)-2-(2-methyl-4-nitro-1H-imidazol-1-yl)may also find applications in material science, where its unique structure could be utilized to develop new materials with specific properties, such as in the creation of advanced polymers or other synthetic materials, subject to further exploration and development.
Check Digit Verification of cas no
The CAS Registry Mumber 79456-89-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,5 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79456-89:
(7*7)+(6*9)+(5*4)+(4*5)+(3*6)+(2*8)+(1*9)=186
186 % 10 = 6
So 79456-89-6 is a valid CAS Registry Number.
79456-89-6Relevant academic research and scientific papers
Sun, Juan,Liu, Han-Yu,Xu, Ruo-Fei,Zhu, Hai-Liang
, p. 6581 - 6588 (2017)
Recent progress in the development of small molecular skeleton-derived polo-like kinase (PLK1) catalytic domain (KD) inhibitors has led to the synthesis of multiple ligands with high binding affinity. However, few systematic analyses have been
CONDENSED IMIDAZO-1,2,4-AZINES. 4. SYNTHESIS OF 1,4-DIHYDROIMIDAZO-1,2,4-TRIAZINE DERIVATIVES
Povstyanoi, M. V.,Klykov, M. A.,Klyuev, N. A.
, p. 622 - 626 (2007/10/02)
The reaction of 2-methyl-4(5)-nitro- and 2-methyl-4(5)-nitro-5(4)-bromoimidazoles with α-haloketones was investigated, during which a number of 1-acylmethyl-substituted 2-methyl-4-nitro- and 2-methyl-4-nitro-5-bromoimidazoles were obtained. 1,4-Dihydro de
