6653-96-9

Basic information

• Product Name: IMIDAZO[1,2-B]PYRIDAZIN-6-AMINE
• Synonyms: IMIDAZO[1,2-B]PYRIDAZIN-6-AMINE;6-Aminoimidazo[1,2-b]pyridazine;6-imidazo[1,2-b]pyridazinamine
• CAS NO: 6653-96-9
• Molecular Formula: C₆H₆N₄
• Molecular Weight: 134.14
• Mol File: 6653-96-9.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• Density: 1.509 g/cm³
• Refractive Index: 1.774
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• CAS DataBase Reference: IMIDAZO[1,2-B]PYRIDAZIN-6-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: IMIDAZO[1,2-B]PYRIDAZIN-6-AMINE(6653-96-9)
• EPA Substance Registry System: IMIDAZO[1,2-B]PYRIDAZIN-6-AMINE(6653-96-9)

Safety Data

• Hazardous Substances Data: 6653-96-9(Hazardous Substances Data)

Usage

General Description

Imidazo[1,2-b]pyridazin-6-amine is a chemical compound from the pyridazines chemical class, characterized by a six-membered heterocyclic ring with two nitrogen atoms. Imidazo[1,2-b]pyridazin-6-amine, identified by its IUPAC name, does not have much data available pertaining to its physical and chemical properties. Information about its applications is also limited, indicating that it may not be widely used in industry or research. Further studies and data collections are required to better understand its characteristics, potential uses, and safety profiles.

InChI:InChI=1/C6H6N4/c7-5-1-2-6-8-3-4-10(6)9-5/h1-4H,(H2,7,9)

Upstream product

• 13526-73-3 6-azido-imidazo[1,2-b]pyridazine 
• 6775-78-6 6-chloroimidazo[1,2-b]pyridazine 
• 13493-79-3 C₆H₄ClN₃*ClH 

Downstream Products

• 316352-12-2 C₂₇H₃₁N₁₁O₉S₂ 
• 159045-46-2 C₂₁H₂₁N₁₁O₇S₂ 
• 316352-11-1 C₂₂H₂₃N₁₁O₇S₂ 
• 166176-43-8 6-(tert-butoxycarbonylaminoacetyl)aminoimidazo[1,2-b]pyridazine 
• 159045-44-0 3-(6-aminoimidazo[1,2-b]pyridazinium-1-yl)methyl-7β-[2-(5-amino-1,2,4-thiadiazol-3-yl)-2(Z)-methoxymethoxyiminoacetamido]-3-cephem-4-carboxylate 
• 159045-51-9 6-ureidoimidazo[1,2-b]pyridazine 
• 316352-03-1 6-N'-methylureidoimidazo[1,2-b]pyridazine 
• 316352-04-2 6-(phthalimidoacetyl)aminoimidazo[1,2-b]pyridazine 

Relevant articles and documents

Mild and highly selective palladium-catalyzed monoarylation of ammonia enabled by the use of bulky biarylphosphine ligands and palladacycle precatalysts

A method for the Pd-catalyzed arylation of ammonia with a wide range of aryl and heteroaryl halides, including challenging five-membered heterocyclic substrates, is described. Excellent selectivity for monoarylation of ammonia to primary arylamines was achieved under mild conditions or at rt by the use of bulky biarylphosphine ligands (L6, L7, and L4) as well as their corresponding aminobiphenyl palladacycle precatalysts (3a, 3b, and 3c). As this process requires neither the use of a glovebox nor high pressures of ammonia, it should be widely applicable.

Cephem compounds, their production and use

Novel cephem compounds of the general formula: STR1 wherein R1 is a lower alkyl group, and salts and esters thereof, showing excellent and balanced antibacterial activity against a broad spectrum of bacteria, especially by rectal administration, and their production and use as antimicrobial agents are described.