27257-90-5 Usage
Description
2,4,6-tris(4-pyrazol-1-yl)-1,3,5-triazine is a nitrogen-containing heterocyclic compound that features a triazine ring with three pyrazolyl substituents. This unique structure endows it with distinctive properties, making it a versatile chemical entity with potential applications in various fields.
Uses
Used in Coordination Chemistry:
2,4,6-tris(4-pyrazol-1-yl)-1,3,5-triazine is utilized as a ligand in coordination chemistry for its ability to form stable complexes with metal ions. Its tridentate nature allows for the creation of complexes with unique geometrical and electronic properties, which can be further explored for various applications.
Used in Metal-Organic Frameworks (MOFs):
In the realm of material science, 2,4,6-tris(4-pyrazol-1-yl)-1,3,5-triazine is employed as a building block for the synthesis of metal-organic frameworks. These MOFs benefit from the compound's structural characteristics, leading to materials with high porosity, large surface areas, and tunable functionalities, which are desirable for applications such as gas storage, catalysis, and drug delivery.
Used in Drug Development:
2,4,6-tris(4-pyrazol-1-yl)-1,3,5-triazine has been investigated for its potential biological activities, making it a candidate for drug development. Its heterocyclic nature and the presence of nitrogen atoms can contribute to its interaction with biological targets, offering a promising avenue for the discovery of new pharmaceutical agents.
Used in the Synthesis of Functional Materials:
2,4,6-tris(4-pyrazol-1-yl)-1,3,5-triazine is also used as a precursor in the synthesis of functional materials. Its incorporation into polymers, dendrimers, or other complex structures can lead to materials with tailored properties for specific applications, such as sensors, optoelectronics, or advanced composites.
Check Digit Verification of cas no
The CAS Registry Mumber 27257-90-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,2,5 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27257-90:
(7*2)+(6*7)+(5*2)+(4*5)+(3*7)+(2*9)+(1*0)=125
125 % 10 = 5
So 27257-90-5 is a valid CAS Registry Number.
27257-90-5Relevant articles and documents
Luminescent complexes of Eu3+,Tb3+ and Gd3+ nitrates with polytopic ligand 2,4,6-tris(1H-pyrazol-1-yl)-1,3,5-triazine
Belousov, Yu. A.,Gontcharenko, V. E.,Kordeyro Magrino, D. A.,Korshunov, V. M.,Lyssenko, K. A.,Pettinari, C.,Taydakov, I. V.
, (2020)
Three novel coordination compounds based on 2,4,6-tris(1H-pyrazolyl)-l,3,5-triazine ligand (PzTz), namely [Ln(PzTz)(NO3)3(H2O)] (Ln = Eu, Gd, Tb) were synthesized and spectroscopically and structurally characterized. X-ray
Copper(II) assisted hydrolysis of 2,4,6-tris(pyrazol-1-yl)-1,3,5-triazine. Crystal and molecular structure of catena-[CuL(H2O)Cl]n (L = 2,4-dione-1,3,5-(1H)-triazin-1-amido)
Manzur, Jorge,Acu?a, Carolina,Vega, Andrés,García, Ana María
, p. 637 - 642 (2011)
This article describes the partial hydrolysis of the multidentate ligand 2,4,6-tris(pyrazol-1-yl)-1,3,5-triazine in the presence of copper(II), to give the anionic ligand 2,4-dione-1,3,5-(1H)-triazin-1-amido, which was isolated as the cupric complex catena-[CuL(H2O)Cl]n, where L is the amido ligand. No other hydrolysis products were isolated or identified. The complex defines a zigzag 1D covalent chain, along the b cell axis, through apical copper-oxygen bonds (Cu-N-C-O?Cu bridges).
Formation of a new 1D coordination polymer by in situ ligand reaction of 2,4,6-tris(pyrazol-1-yl)-1,3,5-s-triazine
Cao, Qiang
, p. 648 - 651 (2013/02/25)
Solvothermal reactions of Zn(NO3)2·6H2O, 1,4-benzenedicarboxylic acid (H2BDC) and 2,4,6-tris(pyrazol-1-yl)-1, 3,5- s-triazine, yielded a new coordination polymer [Zn(BDC)(pz) ·H 2O]n (pz= pyrazole). The in situ methanolysis reaction of 2,4,6-tris(pyrazol-1-yl)-1,3,5-s-triazine with pyrazole and 2,4,6-trismethoxy-1, 3,5-triazine was confirmed by their single-crystal structures. [Zn(BDC)(pz)·H2O]n was characterised by elemental analysis, IR, powder X-ray diffraction, photoluminescence and thermogravimetric analyses.
