Imidazo[1,2-a]pyridin-8-ol


Chemical Name: Imidazo[1,2-a]pyridin-8-ol
CAS Number: 69214-22-8
Product Number: AG005WW3(AGN-PC-0KKQ8U)
Synonyms:
MDL No:
Molecular Formula: C7H6N2O
Molecular Weight: 134.1353

Identification/Properties


Properties
MP:
154-157°
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
134.138g/mol
XLogP3:
1.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
134.048g/mol
Monoisotopic Mass:
134.048g/mol
Topological Polar Surface Area:
37.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
129
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

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Chemical Structure



Imidazo[1,2-a]pyridin-8-ol is a versatile compound widely utilized in chemical synthesis for various applications. This heterocyclic structure serves as a key building block in the creation of pharmaceuticals, agrochemicals, and specialty chemicals. With its unique ring system and functional groups, Imidazo[1,2-a]pyridin-8-ol offers multiple points for further modification and derivatization, making it a valuable tool in the development of new compounds with desired properties.In chemical synthesis, Imidazo[1,2-a]pyridin-8-ol is commonly employed as a precursor in the construction of complex molecular structures. Its rigid and aromatic framework provides stability and rigidity to the final products, which is essential for enhancing their biological activity or physical properties. By introducing specific substituents or functional groups onto the Imidazo[1,2-a]pyridin-8-ol scaffold, chemists can tailor the properties of the resulting molecules to meet specific requirements in drug discovery, material science, or other fields.Furthermore, Imidazo[1,2-a]pyridin-8-ol can participate in various organic reactions such as cross-coupling, oxidation, reduction, and cyclization, allowing for efficient and selective transformations to occur. Its presence in a synthetic route can enable chemists to access diverse chemical space and unlock new possibilities in molecular design and synthesis strategies. Overall, Imidazo[1,2-a]pyridin-8-ol serves as a valuable tool for chemists seeking to expand their synthetic capabilities and explore novel chemical entities with potential applications in various industries.