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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)-

4-acetyl-2,3-dihydroisoindol-1-one

CC(=O)c1cccc2c1CNC2=O Request for Quotation
Chemical Name: 4-acetyl-2,3-dihydroisoindol-1-one
CAS Number: 1021874-48-5
Product Number: AG0006UH(AGN-PC-0J0YDU)
Synonyms:
MDL No:
Molecular Formula: C10H9NO2
Molecular Weight: 175.1840

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Chemical Structure


4-Acetylisoindolin-1-one, a versatile compound in chemical synthesis, serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its unique reactivity and structural properties. When used in organic reactions, this compound's acetyl group can undergo a range of transformations to introduce new functional groups, making it a valuable intermediate in the synthesis of complex organic molecules. Its presence in the molecular structure imparts distinct reactivity, enabling selective modifications and facilitating the formation of diverse chemical bonds. Furthermore, the isoindolinone scaffold of this compound provides a rigid and stable framework, enhancing the overall stability and properties of the final products. With its significant role in advancing chemical synthesis, 4-Acetylisoindolin-1-one continues to be a valuable tool for chemists in the development of innovative compounds across various industries.