171018-16-9

Usage

Uses

Used in Pharmaceutical Industry:
2-(1-methyl-1H-tetrazol-5-yl)pyridine is used as a building block for the synthesis of various pharmaceuticals, leveraging its heterocyclic nature and the presence of the tetrazole ring to create compounds with a wide range of biological activities. This makes it a valuable component in the development of new therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical field, 2-(1-methyl-1H-tetrazol-5-yl)pyridine is utilized as a key component in the synthesis of agrochemicals, where its unique structure and properties can be harnessed to develop effective compounds for crop protection and other agricultural applications.
Used in Medicinal Chemistry and Drug Discovery Research:
2-(1-methyl-1H-tetrazol-5-yl)pyridine is employed as a versatile building block in medicinal chemistry and drug discovery research. Its ability to interact with biological targets and contribute to the creation of compounds with diverse biological activities makes it instrumental in the development of innovative therapeutic agents.

Upstream product

• 33893-89-9 5-(2-pyridyl)-1H-tetrazole 
• 74-88-4 methyl iodide 

Relevant academic research and scientific papers

Syntheses of Chelating Tetrazole-Containing Ligands and Studies of Their Palladium(II) and Ruthenium(II) Complexes

Eleven chelating tetrazole-containing ligands have been synthesized, and their complexes with palladium(II) and ruthenium(II) prepared.Proton n.m.r. spectroscopy, electronic absorption spectroscopy and cyclic voltammetry have been used to study the nature of the metal-ligand interactions in these complexes.The negatively charged tetrazolate group is shown to be a strong electron donor with very different properties to those of the protonated or alkylated tetrazole group.This leads to pH control of the properties of transition metal complexes containing such ligands.

Thermally Activated Delayed Fluorescence in CuI Complexes Originating from Restricted Molecular Vibrations

The mechanism of thermally activated delayed fluorescence (TADF) in molecules in aggregated or condensed solid states has been rarely studied and is not well understood. Nevertheless, many applications of TADF emitters are strongly affected by their lumin

Alkyl tetrazoles as diimine (“diim”) ligands for fac-[Re(diim)(CO)3(L)]-type complexes. Synthesis, characterization and preliminary studies of the interaction with bovine serum albumin

Herein, we report a new family of luminescent Re(I) complexes with general formula fac-[Re(diim)(CO)3L]0/+ in which the role of the diimine-type chelating ligand (diim) is played by alkylated tetrazoles. In particular, the design of