1-(1-benzyl-3,5-dimethylpyrazol-4-yl)ethanone|40570-80-7,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)-

1-(1-benzyl-3,5-dimethylpyrazol-4-yl)ethanone

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Chemical Name:	1-(1-benzyl-3,5-dimethylpyrazol-4-yl)ethanone
CAS Number:	40570-80-7
Product Number:	AG0076HN(AGN-PC-05IZL6)
Synonyms:
MDL No:
Molecular Formula:	C14H16N2O
Molecular Weight:	228.2896

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Chemical Structure

1-(1-Benzyl-3,5-dimethyl-1H-pyrazol-4-yl)ethanone is a versatile compound frequently used in chemical synthesis as a key building block. This compound serves as a valuable intermediate in the production of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties and reactivity. In chemical synthesis, it functions as a precursor for the synthesis of diverse organic compounds, enabling the formation of complex molecular structures through strategic bond formations. Additionally, its substituted pyrazole ring and ketone group offer opportunities for further derivatization, making it a crucial component in the creation of novel compounds with desired properties.