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Ethyl 2,5-dimethylimidazo[1,2-a]pyridine-3-carboxylate is a chemical compound that belongs to the group of imidazo[1,2-a]pyridine-3-carboxylates. It is commonly used in pharmaceutical research and drug development as a building block for the synthesis of various biologically active compounds. This chemical has also been identified as a potential carcinogen and mutagen, and its presence in tobacco smoke has raised concerns about its role in the development of cancer. ethyl 2,5-dimethylimidazo[1,2-a]pyridine-3-carboxylate's structure and reactivity make it an important target for studies into its potential health effects and applications in medicine.
Used in Pharmaceutical Research and Drug Development:
Ethyl 2,5-dimethylimidazo[1,2-a]pyridine-3-carboxylate is used as a building block for the synthesis of various biologically active compounds. Its unique structure and reactivity make it a valuable component in the development of new drugs and pharmaceuticals.
Used in Studies on Health Effects and Applications in Medicine:
Ethyl 2,5-dimethylimidazo[1,2-a]pyridine-3-carboxylate is used as a target for studies into its potential health effects and applications in medicine. Its identification as a potential carcinogen and mutagen, as well as its presence in tobacco smoke, has raised concerns about its role in the development of cancer. Research into ethyl 2,5-dimethylimidazo[1,2-a]pyridine-3-carboxylate can help to better understand its impact on human health and potentially lead to the development of new treatments or preventative measures.

81438-49-5

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81438-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81438-49-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,4,3 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81438-49:
(7*8)+(6*1)+(5*4)+(4*3)+(3*8)+(2*4)+(1*9)=135
135 % 10 = 5
So 81438-49-5 is a valid CAS Registry Number.

81438-49-5Downstream Products

81438-49-5Relevant academic research and scientific papers

Reactions with N-chlorosuccinimide of various 5-methylimidazo[1,2-a]pyridine derivatives with an electron-withdrawing group substituted at the 3-position

Ikemoto, Tomomi,Wakimasu, Mitsuhiro

, p. 99 - 108 (2007/10/03)

Chlorination reactions using N-chlorosuccinimide (NCS) was investigated for various 5-methylimidazo[1,2-a]pyridine derivatives with an electron-withdrawing group substituted at the 3-position. These reactions showed different results, and by examining these, we proposed a reaction mechanism via the appropriate 3-halogenoimidazo[1,2-a]pyridium compounds as the reaction intermediates.

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