90844-35-2

Basic information

• Product Name: 3-AMINO-6-PHENYLTHIOPYRIDAZINE
• Synonyms: 3-AMINO-6-PHENYLTHIOPYRIDAZINE;3-PyridazinaMine, 6-(phenylthio)-;6-(phenylthio)pyridazin-3-amine
• CAS NO: 90844-35-2
• Molecular Formula: C₁₀H₉N₃S
• Molecular Weight: 203.26
• EINECS: 200-001-2
• Mol File: 90844-35-2.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 476.267 °C at 760 mmHg
• Flash Point: 241.838 °C
• Appearance: /
• Density: 1.323 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.689
• CAS DataBase Reference: 3-AMINO-6-PHENYLTHIOPYRIDAZINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-AMINO-6-PHENYLTHIOPYRIDAZINE(90844-35-2)
• EPA Substance Registry System: 3-AMINO-6-PHENYLTHIOPYRIDAZINE(90844-35-2)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 90844-35-2(Hazardous Substances Data)

Usage

General Description

3-AMINO-6-PHENYLTHIOPYRIDAZINE is a chemical compound with the molecular formula C10H8N4S. It is a derivative of pyridazine with an amino group (-NH2) at position 3 and a phenylthio group (-C6H5S) at position 6. 3-AMINO-6-PHENYLTHIOPYRIDAZINE is used in the synthesis of pharmaceuticals and agrochemicals, as well as in research and development. Its chemical properties make it suitable for various applications in the pharmaceutical and agricultural industries. 3-AMINO-6-PHENYLTHIOPYRIDAZINE is known for its potential biological activities and it is commonly used as a building block in the creation of new compounds with desired properties.

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

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

Downstream Products

• 113121-42-9 2-phenyl-6-phenylthioimidazo<1,2-b>pyridazin-3(5H)-one 
• 144449-15-0 2-phenethyl-6-phenylthioimidazo<1,2-b>pyridazine 
• 144449-10-5 2-benzyl-6-phenylthioimidazo<1,2-b>pyridazine 
• 154704-29-7 2-t-butyl-6-(phenylthio)imidazo<1,2-b>pyridazine 
• 142074-18-8 2-methyl-6-(phenylthio)imidazo<1,2-b>pyridazine 
• 141409-26-9 2-phenyl-6-phenylthioimidazo<1,2-b>pyridazine 
• 141409-27-0 2-(4'-methylphenyl)-6-phenylthioimidazo<1,2-b>pyridazine 
• 154704-26-4 3-amino-6-(phenylsulfinyl)pyridazine 
• 154704-27-5 3-amino-6-(phenylsulfonyl)pyridazine 
• 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 
• 142074-19-9 3-benzamidomethyl-2-methyl-6-phenylthioimidazo<1,2-b>pyridazine 

Relevant articles and documents

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.

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.