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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)-

Formamide, N-(3-acetylphenyl)-

O=CNc1cccc(c1)C(=O)C Request for Quotation
Chemical Name: Formamide, N-(3-acetylphenyl)-
CAS Number: 72801-78-6
Product Number: AG003SAG(AGN-PC-0CGFBT)
Synonyms:
MDL No: MFCD00157643
Molecular Formula: C9H9NO2
Molecular Weight: 163.1733

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Chemical Structure


Applying N-(3-Acetylphenyl)formamide in chemical synthesis offers a strategic approach to incorporating diverse functionality into organic molecules. By serving as a versatile building block, this compound enables the introduction of an acetyl group while also providing a reactive amide functionality for further derivatization. Through controlled chemical transformations, N-(3-Acetylphenyl)formamide can be utilized to synthesize a wide range of novel compounds with tailored properties and applications in pharmaceuticals, materials science, and agrochemicals. Its strategic use in synthetic chemistry allows for the systematic design and synthesis of complex molecules with enhanced functionalities, making it a valuable tool for organic chemists seeking to develop innovative compounds for various industrial and scientific applications.