71037-71-3

Basic information

• Product Name: 3-Chloro-6-(1H-imidazol-1-yl)pyridazine
• Synonyms: 3-Chloro-6-(1H-imidazol-1-yl)pyridazine 96%;Albb-005028;3-chloro-6-(1H-imidazol-1-yl)pyridazine(SALTDATA: FREE);1-(6-Chloropyridazin-3-yl)1H-indazole;3-Chloro-6-(1H-imidazol-1-yl)pyridazine96%
• CAS NO: 71037-71-3
• Molecular Formula: C₇H₅ClN₄
• Molecular Weight: 180.6
• Product Categories: blocks;Heterocycles;Imidazoles
• Mol File: 71037-71-3.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 416.4 °C at 760 mmHg
• Flash Point: 205.6 °C
• Appearance: /
• Density: 1.47g/cm³
• Vapor Pressure: 9.26E-07mmHg at 25°C
• Refractive Index: 1.702
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3-Chloro-6-(1H-imidazol-1-yl)pyridazine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Chloro-6-(1H-imidazol-1-yl)pyridazine(71037-71-3)
• EPA Substance Registry System: 3-Chloro-6-(1H-imidazol-1-yl)pyridazine(71037-71-3)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 71037-71-3(Hazardous Substances Data)

Usage

General Description

3-Chloro-6-(1H-imidazol-1-yl)pyridazine is a chemical compound with the molecular formula C7H5ClN4. It is a chlorinated pyridazine derivative that contains an imidazole group. This chemical is used in the synthesis of pharmaceuticals and agrochemicals. It has been studied for its potential as an antifungal and antibacterial agent. The compound has also been investigated for its potential use in the treatment of various diseases and disorders. Its chemical structure and properties make it a valuable intermediate for the development of new drugs and agricultural products.

InChI:InChI=1/C7H5ClN4/c8-6-1-2-7(11-10-6)12-4-3-9-5-12/h1-5H

Upstream product

• 141-30-0 3,6-dichlorpyridazine 
• 122-78-1 phenylacetaldehyde 
• 68-12-2 N,N-dimethyl-formamide 
• 288-32-4 1H-imidazole 

Downstream Products

• 100240-25-3 3-(3,5-dimethylphenoxy)-6-(1 H-imidazol-1-yl)pyridazine 
• 1417455-20-9 3-(1H-imidazol-1-yl)-6-(3-methylphenyl)pyridazine 
• 138803-61-9 1-(6-Imidazol-1-yl-pyridazin-3-yloxy)-3-[2-(2-methoxy-phenoxy)-ethylamino]-propan-2-ol 
• 138803-60-8 1-(6-Imidazol-1-yl-pyridazin-3-yloxy)-3-(2-phenoxy-ethylamino)-propan-2-ol 
• 110696-70-3 2-{2-[Benzyl-(2-phenoxy-ethyl)-amino]-ethyl}-6-imidazol-1-yl-2H-pyridazin-3-one 
• 110696-51-0 6-Imidazol-1-yl-2-[2-(2-phenoxy-ethylamino)-ethyl]-2H-pyridazin-3-one 
• 623581-31-7 C₁₉H₂₁N₅O 

Relevant articles and documents

Selective mono-amination of dichlorodiazines

A mild, easy-to-perform, and versatile method for the formation of aminochlorodiazines from reaction of several types of dichlorodiazines (i.e., pyridazines, pyrimidines, and pyrazines) with primary or secondary amines in ethanol in the presence of trieth

An electrochemical nickel-catalyzed arylation of 3-amino-6- chloropyridazines

3-Amino-6-aryl- and 3-amino-6-heteroarylpyridazines have been obtained in generally good yield using a nickel-catalyzed electrochemical cross-coupling between 3-amino-6-chloropyridazines and aryl or heteroaryl halides at room temperature. Comparative experiments involving classical palladium-catalyzed reactions, such as Suzuki, Stille, or Negishi cross-couplings, reveal that the electrochemical method can constitute a reliable alternative tool for biaryl formation. A possible reaction mechanism is proposed on the basis of electrochemical analyses.

Anti-virally active pyridazinamines

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