90844-35-2

Usage

Uses

Used in Pharmaceutical Industry:
3-AMINO-6-PHENYLTHIOPYRIDAZINE is used as a synthetic intermediate for the development of pharmaceuticals due to its unique chemical structure and potential biological activities. It aids in the creation of novel compounds with therapeutic properties, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 3-AMINO-6-PHENYLTHIOPYRIDAZINE is employed as a key component in the synthesis of agrochemicals. Its chemical properties allow it to be integrated into the development of new pesticides or other agricultural chemicals, enhancing crop protection and yield.
Used in Research and Development:
3-AMINO-6-PHENYLTHIOPYRIDAZINE is utilized as a research compound in various scientific studies and development projects. Its presence in laboratories facilitates the exploration of new chemical reactions, the discovery of new compounds, and the investigation of its potential applications in different fields.

InChI:InChI=1/C10H9N3S/c11-9-6-7-10(13-12-9)14-8-4-2-1-3-5-8/h1-7H,(H2,11,12)

Upstream product

• 99844-36-7 6-(toluene-4-sulfonyl)-pyridazin-3-ylamine 
• 930-69-8 sodium thiophenolate 
• 5469-69-2 6-chloro-pyridazin-3-ylamine 
• 108-98-5 thiophenol 
• 14959-31-0 N-(6-chloropyridazin-3-yl)acetamide 

Downstream Products

• 180900-93-0 2-(4-tert-Butyl-phenyl)-6-phenylsulfanyl-imidazo[1,2-b]pyridazine 
• 180900-91-8 2-Naphthalen-2-yl-6-phenylsulfanyl-imidazo[1,2-b]pyridazine 
• 1173149-91-1 C₁₈H₁₂F₂N₄O₂S 
• 144476-72-2 3-acetamidomethyl-2-phenethyl-6-phenylthioimidazo<1,2-b>pyridazine 
• 144449-27-4 2-benzyl-3-dimethylaminomethyl-6-phenylthioimidazo<1,2-b>pyridazine 
• 144448-83-9 3-methoxy-2-phenethyl-6-phenylthioimidazo<1,2-b>pyridazine 
• 144476-70-0 2-benzyl-3-methoxy-6-phenylthioimidazo<1,2-b>pyridazine 
• 142074-19-9 3-benzamidomethyl-2-methyl-6-phenylthioimidazo<1,2-b>pyridazine 

Relevant academic research and scientific papers

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.

Amide anions as unexpected activating groups in nucleophilic heteroaromatic substitution

Nucleophilic displacement of halide by alkoxide in pyridazines, phthalazines, a thiazole and a thiadiazole is unexpectedly activated by acetamido anion substituents compared to neutral amido and amino substituents.

Imidazopyridazines.II 6-Alkylthio- and 6-Arylthio-3-methoxy-2-phenylimidazopyridazines

A series of 6-alkylthio- and 6-arylthio-3-methoxy-2-phenylimidazopyridazines has been prepared from 6-alkylthio- and 6-arylthio-pyridazin-3-amines through the corresponding 6-alkylthio- and 6-arylthio-2-phenylimidazopyridazin-3(5H)-ones.