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2-(4-Benzylpiperazin-1-yl)-4,6-dimorpholino-1,3,5-triazine is a complex organic compound with the molecular formula C18H26N6O2. It is characterized by a triazine ring, which is a six-membered aromatic ring containing three nitrogen atoms. The compound features a benzyl group attached to the piperazine ring at the 4-position, and two morpholino groups are attached to the triazine ring at the 4 and 6 positions. This structure contributes to its potential applications in various fields, such as pharmaceuticals and agrochemicals, due to its unique chemical properties and the ability to form hydrogen bonds. The compound's synthesis and reactivity are of interest to researchers studying the properties of heterocyclic compounds and their potential uses in drug development and other chemical applications.

21218-55-3

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21218-55-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21218-55-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,1 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21218-55:
(7*2)+(6*1)+(5*2)+(4*1)+(3*8)+(2*5)+(1*5)=73
73 % 10 = 3
So 21218-55-3 is a valid CAS Registry Number.

21218-55-3Downstream Products

21218-55-3Relevant academic research and scientific papers

Synthesis and antibacterial activity of some novel 4-benzyl-piperazinyl-s- triazine derivatives

Jana,Das

, p. 186 - 190 (2013/02/22)

Considerable interest has been attracted in s-triazine scaffold and its derivatives because of their large variety of pharmacological activities. In this project, a series of 4-benzyl-piperazinyl-s-triazine derivatives 5a to 5j were synthesized by three steps substitution reaction of cyanuric chloride with various nucleophilic compounds in presence of a base. Molecular structures of the synthesized compounds were elucidated by FTIR, 1H NMR, 13C NMR, MS spectral data and elemental analyses. The in vivo antibacterial activity was evaluated by broth dilution method against representative four Gram-positive and four Gram-negative bacterial strains. Many compounds have displayed comparable better antibacterial activity against Bacillus subtilis, Staphylococcus aureus, Staphylococcus epidermis and Pseudomonas aeruginosa with reference to streptomycin.

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