6-(4-methoxyphenyl)-2-methyl-7H-imidazo[1,2-a]pyrazin-3-one;hydrochloride


Chemical Name: 6-(4-methoxyphenyl)-2-methyl-7H-imidazo[1,2-a]pyrazin-3-one;hydrochloride
CAS Number: 128322-44-1
Product Number: AG000XZD(AGN-PC-00UR79)
Synonyms:
MDL No:
Molecular Formula: C14H14ClN3O2
Molecular Weight: 291.7329

Identification/Properties


Properties
Storage:
Inert atmosphere;2-8℃;
Computed Properties
Molecular Weight:
291.735g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
291.077g/mol
Monoisotopic Mass:
291.077g/mol
Topological Polar Surface Area:
59.6A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
307
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:
2
Compound Is Canonicalized:
Yes

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NMR Spectrum


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Chemical Structure



6-(4-Methoxyphenyl)-2-methylimidazo[1,2-a]pyrazin-3(7H)-one hydrochloride is an important reagent in chemical synthesis, particularly in the development of pharmaceutical compounds. Its unique structure and reactivity make it a versatile building block for the preparation of various functionalized molecules.This compound is commonly used as a key intermediate in the synthesis of bioactive compounds, such as potential drug candidates and research probes. Its presence in the molecular structure imparts specific properties that can enhance the desired biological activity of the final product.In chemical synthesis, 6-(4-Methoxyphenyl)-2-methylimidazo[1,2-a]pyrazin-3(7H)-one hydrochloride can serve as a valuable starting material for the construction of heterocyclic frameworks or the introduction of specific functional groups through various chemical transformations. Its incorporation into organic molecules can lead to the development of new therapeutic agents or molecular tools for biological studies.Overall, the strategic utilization of 6-(4-Methoxyphenyl)-2-methylimidazo[1,2-a]pyrazin-3(7H)-one hydrochloride in chemical synthesis enables the efficient and targeted preparation of structurally diverse compounds with potential applications in medicinal chemistry and related fields.