3-Bromo-6-ethyl-5-methylpyrazolo[1,5-a]pyrimidin-7(4H)-one|1403767-27-0,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-

O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]

Tris(dibenzylideneacetone)dipalladium

C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C

Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

3-Bromo-6-ethyl-5-methylpyrazolo[1,5-a]pyrimidin-7(4H)-one

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Chemical Name:	3-Bromo-6-ethyl-5-methylpyrazolo[1,5-a]pyrimidin-7(4H)-one
CAS Number:	1403767-27-0
Product Number:	AG001CBE(AGN-PC-0WA8B1)
Synonyms:
MDL No:
Molecular Formula:	C9H10BrN3O
Molecular Weight:	256.0992

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Chemical Structure

3-Bromo-6-ethyl-5-methylpyrazolo[1,5-a]pyrimidin-7(4H)-one, a versatile compound in chemical synthesis, serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure allows for the introduction of functional groups at multiple positions, offering synthetic chemists flexibility in designing and optimizing target molecules. The presence of both bromine and a pyrimidine core makes this compound particularly useful in transition-metal-catalyzed cross-coupling reactions, facilitating the formation of complex molecular structures. Additionally, the ethyl and methyl substituents contribute to the compound's stability and reactivity, broadening its utility in diverse synthetic pathways.