1844-53-7

Basic information

• Product Name: 6-Chloro-2-phenylimidazo[1,2-b]pyridazine
• Synonyms: 6-Chloro-2-phenylimidazo[1,2-b]pyridazine;6-chloro-2-phenyl-imidazo[2,1-f]pyridazine;6-chloro-2-phenylimidazo[2,1-f]pyridazine
• CAS NO: 1844-53-7
• Molecular Formula: C₁₂H₈ClN₃
• Molecular Weight: 229.66
• Mol File: 1844-53-7.mol
• Article Data: 5

Chemical Properties

• Melting Point: 200 °C
• Appearance: /
• Density: 1.353g/cm³
• Refractive Index: 1.69
• PKA: 2.86±0.30(Predicted)
• CAS DataBase Reference: 6-Chloro-2-phenylimidazo[1,2-b]pyridazine(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Chloro-2-phenylimidazo[1,2-b]pyridazine(1844-53-7)
• EPA Substance Registry System: 6-Chloro-2-phenylimidazo[1,2-b]pyridazine(1844-53-7)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 1844-53-7(Hazardous Substances Data)

Usage

General Description

6-Chloro-2-phenylimidazo[1,2-b]pyridazine, also known as CL-II-49, is a chemical compound with the molecular formula C11H7ClN4. It is a heterocyclic compound that contains a chlorine atom and a phenyl group. This chemical has been studied for its potential medicinal properties, including its use as an antitumor agent and its ability to inhibit the growth of cancer cells. Additionally, it has been investigated for its potential as a therapeutic treatment for diseases such as malaria and as an anti-inflammatory agent. The compound's structure and properties make it a promising candidate for further research and development in the pharmaceutical industry.

InChI:InChI=1/C12H8ClN3/c13-11-6-7-12-14-10(8-16(12)15-11)9-4-2-1-3-5-9/h1-8H

Upstream product

• 1023697-90-6 6-chloro-3-iodo-2-phenylimidazo[1,2-b]pyridazine 
• 107-19-7 propargyl alcohol 
• 17997-47-6 2-tri-n-butylstannylpyridine 
• 5469-69-2 6-chloro-pyridazin-3-ylamine 
• 70-11-1 α-bromoacetophenone 
• 1945-84-2 2-ethynylpyridine 
• 65610-18-6 6-chloro-1-oxy-2-phenyl-imidazo[1.2-b]pyridazine 

Downstream Products

• 1844-61-7 6-methoxy-2-phenylimidazo<1,2-b>pyridazine 
• 1023698-07-8 C₁₉H₁₆N₄O 
• 1023697-90-6 6-chloro-3-iodo-2-phenylimidazo[1,2-b]pyridazine 
• 944902-75-4 2-bromo-6-chloroimidazo[1,2-b]pyridazine 
• 1105714-42-8 2-(3,5-difluorophenyl)-3-pyridazin-4-yl-6-(4-pyrrolidin-1-yl-piperidin-1-yl)-imidazo[1,2-b]pyridazine 
• 1105714-15-5 6-(4-isopropylpiperazin-1-yl)-2-phenyl-3-pyridazin-4-yl-imidazo[1,2-b]pyridazine 
• 1105714-52-0 6-chloro-2-phenyl-3-(pyridazin-4-yl)imidazo[1,2-b]pyridazine 
• 1105714-51-9 ethyl 4-[6-chloro-2-phenylimidazo[1,2-b]pyridazin-3-yl]-4H-pyridazine-1-carboxylate 
• 1220351-58-5 6-chloro-3-(4-nitrophenyl)-2-phenylimidazo[1,2-b]pyridazine 

Relevant articles and documents

Organic electroluminescence compound based on imidazole and pyridazine as well as application and organic electroluminescence device thereof

The invention provides an organic electroluminescence compound based on imidazole and pyridazine. The organic electroluminescence compound has the following structure as shown in the description. Thecompound has relatively good heat stability, high luminescence efficiency and high luminescence purity and can be applied to the organic electroluminescence devices, organic solar cells, organic thin-film transistors or organic photoreceptors. The invention also provides an organic electroluminescence device. The device comprises an anode, a cathode and an organic layer, wherein the organic layercomprises at least one luminescence layer, a hole injection layer, a hole transport layer, a hole barrier layer, an electron injection layer and an electron transport layer, and at least one layer ofthe organic layers comprises the compound of the structural formula I. The organic electroluminescence device produced by adopting the organic electroluminescence compound has the advantages of good electroluminescence efficiency, excellent color purity and long service life.

Nitrogen heterocyclic compound, application thereof and OLED (organic light-emitting device)

The invention provides a nitrogen heterocyclic compound with a structural formula shown in the description. The nitrogen heterocyclic compound has better heat stability, high light-emitting efficiencyand high light-emitting purity and can be applied to th

Studies on Heterocyclic Compounds. XXII. The Reaction of Oxazolopyridazinium Perchlorates with Hydroxylamines

The reaction of oxazolopyridazinium perchlorates (I) with hydroxylamine hydrochloride and potassium hydroxide in N,N-dimethylformamide afforded 2-(2,3-dihydro-3-hydroxyimino-2-pyridazinyl)ethanones (II) and 2-(2,3-dihydro-3-hydroxyimino-2-pyridazin