Imidazo[1,2-a]pyridine-3-carboxylic acid, 6-bromo-, ethyl ester


Chemical Name: Imidazo[1,2-a]pyridine-3-carboxylic acid, 6-bromo-, ethyl ester
CAS Number: 372198-69-1
Product Number: AG00BZJL(AGN-PC-03JD2G)
Synonyms:
MDL No:
Molecular Formula: C10H9BrN2O2
Molecular Weight: 269.0947

Identification/Properties


Properties
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
269.098g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
267.985g/mol
Monoisotopic Mass:
267.985g/mol
Topological Polar Surface Area:
43.6A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
250
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 6-bromoimidazo[1,2-a]pyridine-3-carboxylate is commonly utilized in chemical synthesis as a versatile building block and intermediate. Its unique structure and reactivity make it valuable for the preparation of various functionalized heterocyclic compounds and pharmaceutical agents. In organic transformations, Ethyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylate serves as a key starting material for the synthesis of biologically active molecules, including antiviral, antibacterial, and anticancer agents. Its strategic incorporation in synthetic routes enables the efficient construction of complex molecular frameworks with specific pharmacological properties. Additionally, the substitution and functionalization of the bromo and carboxylate groups on the imidazo[1,2-a]pyridine ring allow for the modulation of the compound's physicochemical characteristics and biological activities, further expanding its synthetic utility in drug discovery and medicinal chemistry research.