27257-90-5

Basic information

• Product Name: 2,4,6-tris(4-pyrazol-1-yl)-1,3,5-triazine
• Synonyms: 2,4,6-tris(4-pyrazol-1-yl)-1,3,5-triazine
• CAS NO: 27257-90-5
• Molecular Formula: C₁₂H₉N₉
• Molecular Weight: 369.3381
• Mol File: 27257-90-5.mol
• Article Data: 8

Chemical Properties

• Melting Point: 238-239 °C(Solv: ethyl acetate (141-78-6))
• Boiling Point: 629.9±38.0 °C(Predicted)
• Appearance: /
• Density: 1.61±0.1 g/cm3(Predicted)
• PKA: -0.71±0.19(Predicted)
• CAS DataBase Reference: 2,4,6-tris(4-pyrazol-1-yl)-1,3,5-triazine(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-tris(4-pyrazol-1-yl)-1,3,5-triazine(27257-90-5)
• EPA Substance Registry System: 2,4,6-tris(4-pyrazol-1-yl)-1,3,5-triazine(27257-90-5)

Safety Data

• Hazardous Substances Data: 27257-90-5(Hazardous Substances Data)

Usage

General Description

2,4,6-tris(4-pyrazol-1-yl)-1,3,5-triazine is a chemical compound that consists of a triazine ring with three pyrazolyl substituents. It is a nitrogen-containing heterocyclic compound and can be used in various applications due to its unique structure and properties. It has been studied for its potential use in coordination chemistry, as a ligand in metal-organic frameworks, and as a building block for the synthesis of functional materials. 2,4,6-tris(4-pyrazol-1-yl)-1,3,5-triazine has also been investigated for its potential biological activities and as a potential candidate for drug development. Overall, 2,4,6-tris(4-pyrazol-1-yl)-1,3,5-triazine is a versatile and valuable chemical compound with diverse potential applications.

Upstream product

• 288-13-1 NH-pyrazole 
• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 10199-67-4 1-benzylpyrazole 

Downstream Products

• 1418029-85-2 Zn⁽²⁺⁾*C₈H₄O₄^(2-)*C₃H₄N₂*H₂O 
• 877-89-4 2,4,6-trimethoxy-1,3,5-triazine 

Relevant 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

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)

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

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.