107599-30-4

Usage

Uses

Used in Coordination Chemistry:
3,6-bis(pyridin-3-yl)-1,2,4,5-tetrazole is utilized as a ligand in coordination chemistry for its ability to form stable complexes with metal ions. Its nitrogen-rich structure contributes to its strong affinity for metals, making it a valuable component in the design of coordination compounds with specific properties and applications.
Used in Material Science:
In material science, 3,6-bis(pyridin-3-yl)-1,2,4,5-tetrazole is employed as a building block for the development of new materials with tailored properties. Its incorporation into materials can lead to enhanced performance in areas such as conductivity, stability, and reactivity.
Used in Catalysis:
3,6-bis(pyridin-3-yl)-1,2,4,5-tetrazole serves as a catalyst or a catalyst support in various chemical reactions. Its unique electronic and steric properties allow it to facilitate and enhance the rates of reactions, making it a useful component in catalytic processes.
Used in Organic Synthesis:
As an intermediate in organic synthesis, 3,6-bis(pyridin-3-yl)-1,2,4,5-tetrazole is used to synthesize a range of organic compounds. Its reactivity and functional groups make it a versatile component in the construction of complex organic molecules.
Used in Medicinal Chemistry:
3,6-bis(pyridin-3-yl)-1,2,4,5-tetrazole is explored in medicinal chemistry as a potential candidate for the development of new pharmaceuticals. Its biological activity and ability to interact with biological targets make it a promising compound for creating novel therapeutic agents.
Used in the Construction of Complex Molecular Architectures:
In supramolecular chemistry, 3,6-bis(pyridin-3-yl)-1,2,4,5-tetrazole is used as a building unit for the assembly of complex molecular structures. Its ability to form multiple non-covalent interactions, such as hydrogen bonding and π-π stacking, contributes to the stability and functionality of the resulting architectures.

Upstream product

• 31599-23-2 3,6-bis(3'-pyridyl)-1,2-dihydro-1,2,4,5-tetrazine 
• 100-54-9 pyridine-3-carbonitrile 

Downstream Products

• 31599-23-2 3,6-bis(3'-pyridyl)-1,4-dihydro-1,2,4,5-tetrazine 
• 1224741-58-5 C₃₄H₂₂N₈ 
• 1224741-61-0 C₄₈H₃₀N₁₂ 
• 1224741-55-2 4-phenyl-3,6-di(pyridine-3-yl)pyridazine 

Relevant academic research and scientific papers

H-bond mediated self-assembly 1-dimensional array of 3,6-Bis(3′- Pyridyl)-1,2,4,5-tetrazine with trimesic acid

3,6-Bis(3'-pyridyl)-l,2,4,5-tetrazine was prepared by reaction of 3-cyanopyridine with hydrazine. Slow evaporation of 3,6-bis(3′-pyridyl)-l, 2,4,5-tetrazine with trimesic acid, in a 2:1 molar ratio in methanol afforded single crystals of 1 C33H22N12O6, suitable for X-ray analysis. The product was characterized by spectroscopic and single-crystal X-ray diffraction studies. The hydrogen bond mediated self-assembly of 3,6-bis(3'-pyridyl)-l,2,4,5-tetrazine with trimesic acid molecules generates 1-dimensional multi-compartmental arrays in the solid state as revealed by X-ray crystallographic analysis. The crystal structure of 1 is monoclinic with a = 28.445(3), b = 6.7088(10), c = 33.846(4) A, a = 90°, β= 108.112(7°, γ -90°, Z = 8, and space group C2/c. The directional intermodular hydrogen bonding between 3,6-bis(3′-pyridyl)- 1,2,4,5-tetrazine and trimesic acid molecules uses O-H...N and C-H...O interactions, together with intramolecular C-H...N hydrogen bonding, to build up the one-dimensional network structure.

Novel 3,6-unsymmetrically disubstituted-1,2,4,5-tetrazines: S-induced one-pot synthesis, properties and theoretical study

18 unprecedented tetrazines unsymmetrically substituted at C3 and C6 by an aromatic heterocycle have been successfully prepared by the S-induced reaction of aromatic nitriles with hydrazine hydrate under thermal conditions. The spectral property investiga

ADDITIVE FOR IMPARTING LOW HEAT BUILD-UP TO RUBBER COMPONENT

Provided is an additive for imparting low heat build-up to a rubber component, wherein the additive includes a tetrazine compound represented by general formula (1): (wherein X1 and X2 are the same or different and represent a hydrogen atom or an alkyl, alkylthio, aralkyl, aryl, arylthio, heterocyclic, or amino group; and each of these groups may have one or more substituents), or a salt thereof.

Modification of 1,2,4,5-tetrazine with cationic rhenium(i) polypyridine units to afford phosphorogenic bioorthogonal probes with enhanced reaction kinetics

New phosphorogenic bioorthogonal probes derived from mononuclear and binuclear rhenium(i) polypyridine complexes containing a 1,2,4,5-tetrazine moiety were designed; these complexes displayed substantial dienophile-induced emission enhancement, and accelerated reaction kinetics and could target a protein conjugate in living cells.