3H-imidazo[4,5-b]pyridine


Chemical Name: 3H-imidazo[4,5-b]pyridine
CAS Number: 273-21-2
Product Number: AG00BBYZ(AGN-PC-0BT47U)
Synonyms:
MDL No:
Molecular Formula: C6H5N3
Molecular Weight: 119.1240

Identification/Properties


Computed Properties
Molecular Weight:
119.127g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
119.048g/mol
Monoisotopic Mass:
119.048g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
105
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



3H-Imidazo[4,5-b]pyridine is a versatile heterocyclic compound that finds extensive application in chemical synthesis due to its unique structural properties and reactivity. One key area where 3H-Imidazo[4,5-b]pyridine is utilized is in pharmaceutical research and drug development. Its scaffold serves as a core structure in the synthesis of various biologically active molecules, particularly in the design of novel therapeutic agents. The presence of nitrogen atoms in the heterocycle allows for the introduction of diverse functional groups, enabling the modification of its properties to enhance biological activity or optimize pharmacokinetic profiles.In addition to its role in drug discovery, 3H-Imidazo[4,5-b]pyridine is also employed in the synthesis of agrochemicals and advanced materials. Its ability to undergo various chemical transformations, such as cross-coupling reactions and cyclization processes, makes it a valuable building block for the construction of complex organic molecules with specific functionalities. Furthermore, the presence of the imidazo ring system imparts unique electronic and steric properties to the compound, influencing its reactivity and interactions in diverse synthetic pathways.Overall, 3H-Imidazo[4,5-b]pyridine serves as a versatile substrate in chemical synthesis, facilitating the creation of structurally diverse compounds with potential applications in pharmaceuticals, agrochemicals, and materials science.