6285-28-5

Usage

Uses

Used in Pharmaceutical Industry:
3,5-DIETHYL-1,2,4-TRIAZOL-4-YLAMINE is used as a building block for the synthesis of pharmaceutical drugs due to its versatile molecular structure and compatibility in various chemical reactions. Its potential biological activities and medicinal properties make it a valuable component in the development of new therapeutic agents.
Used in Agricultural Industry:
In the agricultural sector, 3,5-DIETHYL-1,2,4-TRIAZOL-4-YLAMINE is utilized as a building block for the synthesis of agrochemicals. Its chemical properties allow it to be incorporated into the development of new pesticides, herbicides, and other agricultural chemicals to improve crop protection and yield.
Used in Organic Synthesis:
3,5-DIETHYL-1,2,4-TRIAZOL-4-YLAMINE is used as a versatile compound in organic synthesis processes. Its molecular structure enables it to participate in a wide range of chemical reactions, making it a valuable component in the creation of various organic compounds for research and industrial applications.
Used in Research and Development:
3,5-DIETHYL-1,2,4-TRIAZOL-4-YLAMINE is employed as a subject of research and development in both pharmaceutical and agricultural fields. Its potential biological activities and medicinal properties are of interest to scientists and researchers who aim to explore its full potential and unlock new applications for 3,5-DIETHYL-1,2,4-TRIAZOL-4-YLAMINE.

InChI:InChI=1/C6H12N4/c1-3-5-8-9-6(4-2)10(5)7/h3-4,7H2,1-2H3

Upstream product

• 802294-64-0 propionic acid 
• 107-12-0 propiononitrile 
• 10076-48-9 methyl 2,2-dimethoxypropionate 
• 1528-34-3 N¹,N²-dipropionylhydrazine 

Downstream Products

• 80510-86-7 4-Chloro-N-(3,5-diethyl-[1,2,4]triazol-4-yl)-benzamidine 
• 1421023-54-2 C₃₂H₄₂N₈O₅ 
• 1421023-53-1 C₃₂H₄₂N₈O₅ 
• 1421161-67-2 (N,N',N,N')-N,N'-(4,4'-(butane-1,4-diylbis(oxy))bis(4,1-phenylene))bis(methan-1-yl-1-ylidene)bis(3,5-diethyl-4H-1,2,4-triazol-4-amine) 
• 1421161-69-4 C₃₀H₄₂N₈O₂ 
• 1421161-65-0 (N,N',N,N')-N,N'-(2,2'-(butane-1,4-diylbis(oxy))bis(2,1-phenylene))bis(methan-1-yl-1-ylidene)bis(3,5-diethyl-4H-1,2,4-triazol-4-amine) 
• 122583-44-2 (3,5-Diethyl-[1,2,4]triazol-1-yl)-[1-phenyl-meth-(E)-ylidene]-amine 

Relevant academic research and scientific papers

4-Amino-3,5-diethyl-4H-1,2,4-triazole at 100 K: Chains of edge-fused R 44(10) and R44(20) rings

The title compound, C6H12N4, has four crystallographically independent mol-ecules in the asymmetric unit. Inter-molecular N - H...N hydrogen bonds involving amino groups and triazole N atoms form a three-dimensional framework involving R 4 4(10) and R 4 4(20) rings. The hydrogen bonding is supported by weak C - H...π inter-actions. International Union of Crystallography 2007.

Process for the synthesis of 4-amino-1,2,4-(4h)triazole derivatives

A process for preparing a 4-amino-1,2,4-(4H)triazole derivative compositions having the formula STR1 wherein R is hydrogen or an alkyl group containing from 1 to about 10 carbon atoms, which alkyl group can be additionally substituted by one or more aryl, heteroaryl, hydroxy, or alkenyl substituents, comprising the step of reacting hydrazine or an aqueous hydrazine solution with a carboxylic acid having the formula RCO2 H in the presence of an insoluble polymer containing acidic functional groups sufficiently strong to cause the reaction to proceed under mild conditions to produce a product of high yield and purity.

Synthesis of 3,5-biscarbonyl-1H-1,2,4-triazole derivatives

The hitherto unreported 1H-1,2,4-triazole-3,5-dicarbaldehyde can be prepared in three steps by condensation of methyl dimethoxyacetate with hydrazine, followed by oxidative deamination and deacetalization.