39614-78-3

Usage

Uses

Used in Pharmaceutical Research and Development:
6-Ethoxypyridazin-3-amine is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it a valuable building block in the creation of novel drug candidates, particularly in the fields of medicinal chemistry and drug discovery.
Used in Organic Synthesis:
In the field of organic synthesis, 6-Ethoxypyridazin-3-amine serves as a versatile intermediate. It can be employed to produce a range of other organic compounds, contributing to the development of new chemical entities with potential applications in various industries.
Used in Scientific Research:
6-Ethoxypyridazin-3-amine is utilized in scientific research to explore its chemical properties, reactivity, and potential interactions with biological systems. This research can lead to a better understanding of its applications and the discovery of new uses in various scientific and industrial fields.
Overall, 6-Ethoxypyridazin-3-amine is a promising chemical compound with a wide range of potential applications in pharmaceuticals, organic synthesis, and scientific research, driven by its unique structural properties and reactivity.

InChI:InChI=1/C6H9N3O/c1-2-10-6-4-3-5(7)8-9-6/h3-4H,2H2,1H3,(H2,7,8)

Upstream product

• 5469-69-2 6-chloro-pyridazin-3-ylamine 
• 141-52-6 sodium ethanolate 
• 64-17-5 ethanol 

Downstream Products

• 1844-66-2 6-ethoxy-2-phenylimidazo<1,2-b>pyridazine 
• 184015-10-9 6-Ethoxy-2-p-tolyl-imidazo[1,2-b]pyridazine 
• 1844-68-4 2-(4-chlorophenyl)-6-ethoxyimidazo<1,2-b>pyridazine 
• 1173149-86-4 C₁₄H₁₂F₂N₄O₃ 

Relevant academic research and scientific papers

2-Phenylimidazo[1,2-b]pyridazine derivatives highly active against Haemonchus contortus

A series of 2-phenylimidazo[1,2-b]pyridazine derivatives were synthesized and evaluated for their in vitro anthelmintic activity against Haemonchus contortus. The most active compounds had in vitro LD99 values of 30 nM, which is comparable to that of the benchmark commercial nematocide, Ivermectin.

Design, synthesis, and bioactivity study of novel benzoylpyridazyl ureas

A series of novel benzoylpyridazyl ureas were designed and synthesized from maleic anhydride and hydrazine monohydrate. These benzoylureas were identified by 1H NMR spectroscopy and element analysis. The bioactivities of the new compounds were evaluated. These compounds exhibited larvicidal activities against oriental armyworm, and in particular, compound 13 displayed comparable activity to the commercial insecticide Hexaflumuron. Most of these compounds also had some larvicidal activities against mosquito. Interestingly, some compounds showed good plant growth regulatory activities.

A revision of the alcoholysis and alkanethiolysis of 3-amino-6-chloropyridazine

The synthesis of 3-amino-6-alkoxy- and 3-amino-6-alkylthiopyridazines via nucleophilic aromatic substitution on 3-amino-6-chloropyridazine is described. In contrast to literature reports, no pressure tube is required to perform these reactions.