202348-55-8 Usage
Uses
Used in Chemical Synthesis:
Imidazo[1,2-a]pyridine-2-carboxaldehyde, 6-methyl(9CI) is used as a building block in the synthesis of organic molecules. Its unique molecular structure allows for the creation of a wide range of compounds with diverse properties and applications.
Used in Pharmaceutical Applications:
Imidazo[1,2-a]pyridine-2-carboxaldehyde, 6-methyl(9CI) is utilized in the development of new drugs. Its potential biological activities make it a valuable compound for research and drug discovery. It may contribute to the creation of innovative therapeutic agents with novel mechanisms of action.
Used in Chemical Reactions:
Imidazo[1,2-a]pyridine-2-carboxaldehyde, 6-methyl(9CI) serves as a reagent in various chemical reactions. Its aldehyde functional group enables it to participate in a range of reactions, such as condensation, oxidation, and reduction, facilitating the synthesis of complex organic molecules.
Used in Research and Development:
Imidazo[1,2-a]pyridine-2-carboxaldehyde, 6-methyl(9CI) is employed as a research tool in the study of biological systems. Its potential interactions with biological molecules and its ability to modulate biological processes make it a valuable compound for understanding the mechanisms underlying various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 202348-55-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,3,4 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 202348-55:
(8*2)+(7*0)+(6*2)+(5*3)+(4*4)+(3*8)+(2*5)+(1*5)=98
98 % 10 = 8
So 202348-55-8 is a valid CAS Registry Number.
202348-55-8Relevant articles and documents
Diversity-Oriented Synthesis of β-Lactams and γ-Lactams by Post-Ugi Nucleophilic Cyclization: Lewis Acids as Regioselective Switch
Li, Zhenghua,Sharma, Upendra Kumar,Liu, Zhen,Sharma, Nandini,Harvey, Jeremy N.,Van Der Eycken, Erik V.
supporting information, p. 3957 - 3962 (2015/06/30)
Heterocyclic fused α-methylene β-lactams were successfully synthesized by a post-Ugi InIII-catalyzed intramolecular addition reaction. Switching from InCl3 to AlCl3 led to the regioselective synthesis of α,β-unsaturated γ-lactams. Moreover, replacing terminal alkynes by substituted alkynes in the Ugi adducts resulted in the exclusive formation of γ-lactams with both catalytic systems. A regioselective approach for the synthesis of heterocyclic fused α-methylene β-lactams and α,β-unsaturated γ-lactams by employing a Ugi reaction followed by InIII- or AlIII-catalyzed intramolecular nucleophilic addition is reported.
CHEMICAL COMPOUNDS 637
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Page/Page column 424-425, (2008/12/07)
The present invention provides a compound of a formula (I), wherein the variables are defined herein; to a process for preparing such a compound; and to the use of such a compound in the treatment of a PDE4 mediated disease state.
