29096-60-4

Basic information

• Product Name: 3-ACETYL-2-METHYLIMIDAZO[1,2-A]PYRIDINE
• Synonyms: BUTTPARK 15\05-98;1-(2-METHYLIMIDAZO[1,2-A]PYRIDIN-3-YL)-1-ETHANONE;3-ACETYL-2-METHYLIMIDAZO[1,2-A]PYRIDINE;1-(2-MethyliMidazo[1,2-a]pyridin-3-yl)ethanone;1-(2-methyl-3-imidazo[3,2-a]pyridinyl)ethanone;1-(2-methylimidazo[3,2-a]pyridin-3-yl)ethanone
• CAS NO: 29096-60-4
• Molecular Formula: C₁₀H₁₀N₂O
• Molecular Weight: 174.2
• Product Categories: Heterocycle-Pyridine series
• Mol File: 29096-60-4.mol
• Article Data: 24

Chemical Properties

• Melting Point: 112
• Appearance: /
• Density: 1.18g/cm³
• Refractive Index: 1.608
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 3-ACETYL-2-METHYLIMIDAZO[1,2-A]PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-ACETYL-2-METHYLIMIDAZO[1,2-A]PYRIDINE(29096-60-4)
• EPA Substance Registry System: 3-ACETYL-2-METHYLIMIDAZO[1,2-A]PYRIDINE(29096-60-4)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 29096-60-4(Hazardous Substances Data)

Usage

General Description

3-Acetyl-2-methylimidazo[1,2-a]pyridine, also known as AIMP, is a chemical compound that belongs to the class of heterocyclic aromatic compounds. It is a potent mutagen and a known carcinogen found in various processed and cooked meats. AIMP is formed during the cooking or processing of animal products, particularly at high temperatures. Studies have shown that exposure to AIMP can lead to DNA damage and increase the risk of developing certain types of cancer, particularly in the colon and prostate. As a result, there is a growing concern about the potential health risks associated with the consumption of foods containing this compound, and efforts are underway to minimize its presence in processed and cooked meats.

InChI:InChI=1/C10H10N2O/c1-7-10(8(2)13)12-6-4-3-5-9(12)11-7/h3-6H,1-2H3

Upstream product

• 504-29-0 2-aminopyridine 
• 1694-29-7 3-chloropentane-2,4-dione 
• 71-43-2 benzene 
• 123-54-6 acetylacetone 
• 30489-51-1 3-(1-hydroxyethyl)-2-methylimidazo<1,2-a>pyridine 
• 30384-93-1 2-metilimidazo<1,2-a>piridin-3-carbossaldeide 
• 934-37-2 2-methylimidazo[1,2-a]pyridine 
• 5231-96-9 N-(2-pyridyl)acetamide 
• 3043-28-5 3-bromopentane-2,4-dione 
• 7732-18-5 water 

Downstream Products

• 1357155-88-4 C₁₇H₁₃N₃O₃ 
• 1164485-41-9 C₁₇H₁₃FN₂O 
• 1357155-82-8 C₁₇H₁₂Cl₂N₂O 

Relevant articles and documents

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Metal free coupling of heteroaryl N-tosylhydrazones and thiols: Efficient synthesis of sulfides

A metal free coupling of heteroaromatic N-tosylhydrazones with thiols is presented. A convenient synthetic route to synthesize heteroaryl N-tosylhydrazones is also showed. Valuable thioethers with pyrroles, pyridines, thieno[2,3-b]pyridines, imidazo[1,2-a]pyridines, and 6H-thieno[2,3-b]pyrroles derivatives were synthesized in good yields. This coupling reaction can be carried out in a one-pot fashion and scaled up to the gram scale by using heteroaryl aldehydes, without the need to isolate the N-tosylhydrazone.