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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
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)-

5(4H)-Isoxazolone, 3-methyl-

O=C1ON=C(C1)C Request for Quotation
Chemical Name: 5(4H)-Isoxazolone, 3-methyl-
CAS Number: 1517-96-0
Product Number: AG007E0J(AGN-PC-0JSI4C)
Synonyms:
MDL No:
Molecular Formula: C4H5NO2
Molecular Weight: 99.0880

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Chemical Structure


In chemical synthesis, 3-Methyl-5(4H)-isoxazolone acts as a versatile building block that can be utilized for the construction of various heterocyclic compounds. With its unique structure, this compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other biologically active molecules. Its reactivity allows for the introduction of diverse functional groups, enabling chemists to access a wide range of structurally complex compounds. Additionally, 3-Methyl-5(4H)-isoxazolone's compatibility with a variety of reaction conditions makes it a valuable tool in the design and development of novel organic transformations. By incorporating this compound into synthetic routes, chemists can expedite the synthesis of target molecules with efficiency and precision.