5367-58-8 Usage
Uses
Used in Pharmaceutical Industry:
5-NITRO-2-PIPERIDIN-1-YL-PHENYLAMINE is used as an active pharmaceutical ingredient for the development of drugs targeting bacterial infections and cancer treatment. Its potent antibacterial properties make it effective against a range of bacterial strains, while its antitumor properties have been studied for potential use in treating various types of cancer.
Used in Agrochemical Industry:
In the agrochemical industry, 5-NITRO-2-PIPERIDIN-1-YL-PHENYLAMINE is used as a key component in the formulation of pesticides and herbicides. Its broad-spectrum activity against various pests and weeds contributes to enhanced crop protection and yield.
Used in Cancer Research:
5-NITRO-2-PIPERIDIN-1-YL-PHENYLAMINE is used as a research tool in cancer research for studying the mechanisms of tumor growth and progression. Its inhibitory effects on various enzymes and biological processes involved in cancer development provide valuable insights into potential therapeutic targets and strategies for cancer treatment.
Used in Enzyme Inhibition Studies:
As a research tool, 5-NITRO-2-PIPERIDIN-1-YL-PHENYLAMINE is used in enzyme inhibition studies to understand the role of specific enzymes in various biological processes. Its ability to inhibit enzymes can help researchers identify potential drug targets and develop novel therapeutic agents for various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 5367-58-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,6 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5367-58:
(6*5)+(5*3)+(4*6)+(3*7)+(2*5)+(1*8)=108
108 % 10 = 8
So 5367-58-8 is a valid CAS Registry Number.
5367-58-8Relevant academic research and scientific papers
Synthesis of quinoxaline derivatives from substituted acetanilides through intramolecular quaternization reactions
De Castro, Sonia,Chicharro, Roberto,Aran, Vicente J.
, p. 790 - 802 (2007/10/03)
The cyclization of 2-dialkylamino-2′-halogeno- and 2-chloro-2′-(dialkylamino)acetanilides to quinoxaline derivatives has been studied in detail. These reactions proceed, respectively, through intramolecular aromatic nucleophilic or aliphatic nucleophilic
