Imidazo[1,2-a]pyridine-2-carboxylic acid, 5-methyl-, ethyl ester


Chemical Name: Imidazo[1,2-a]pyridine-2-carboxylic acid, 5-methyl-, ethyl ester
CAS Number: 67625-35-8
Product Number: AG006CSK(AGN-PC-0JWK1L)
Synonyms:
MDL No:
Molecular Formula: C11H12N2O2
Molecular Weight: 204.2252

Identification/Properties


Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
204.229g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
204.09g/mol
Monoisotopic Mass:
204.09g/mol
Topological Polar Surface Area:
43.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
245
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum


Other Analytical Data


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Chemical Structure



Ethyl 5-methylimidazo[1,2-a]pyridine-2-carboxylate is a valuable compound widely utilized in chemical synthesis for its unique properties and versatile applications. This heterocyclic compound plays a crucial role as a building block in the synthesis of various pharmaceuticals, agrochemicals, and organic materials. Its presence in the molecular structure imparts specific functional groups and structural motifs necessary for the development of biologically active compounds.In organic synthesis, Ethyl 5-methylimidazo[1,2-a]pyridine-2-carboxylate serves as a key intermediate in the preparation of diverse N-heterocycles and fused ring systems. Its structural features enable the formation of complex molecules through strategic bond formations and functional group manipulations. This compound is particularly valuable in the design and production of drug candidates, pesticides, and novel materials with tailored properties.Furthermore, Ethyl 5-methylimidazo[1,2-a]pyridine-2-carboxylate exhibits reactivity that enables facile transformations in synthetic routes, facilitating the assembly of intricate molecular architectures. Its inclusion in synthetic schemes allows for efficient and selective manipulation of chemical bonds, enabling the production of target compounds with high yields and purity.Overall, the application of Ethyl 5-methylimidazo[1,2-a]pyridine-2-carboxylate in chemical synthesis is instrumental in the creation of structurally diverse and functionally rich compounds with potential implications in the fields of medicine, agriculture, and materials science.