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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)-

2(3H)-Benzoxazolone, 6-(3-chloro-1-oxopropyl)-

ClCCC(=O)c1ccc2c(c1)oc(=O)[nH]2 Request for Quotation
Chemical Name: 2(3H)-Benzoxazolone, 6-(3-chloro-1-oxopropyl)-
CAS Number: 132383-36-9
Product Number: AG0010MU(AGN-PC-00G860)
Synonyms:
MDL No:
Molecular Formula: C10H8ClNO3
Molecular Weight: 225.6284

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-(3-Chloropropanoyl)benzo[d]oxazol-2(3H)-one is a versatile compound with valuable applications in chemical synthesis. This compound serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Through its reactive functional groups, such as the chloropropanoyl and oxazolone moieties, this compound can participate in a variety of synthetic transformations to introduce specific functionalities into target molecules. In organic synthesis, it can be utilized as an acylating agent to introduce the 3-chloropropanoyl group into a range of nucleophiles, enabling the synthesis of diverse derivatives. Furthermore, the presence of the benzo[d]oxazol-2(3H)-one scaffold provides opportunities for further elaboration through cyclization, annulation, or modification of the heterocyclic ring system. Overall, the strategic incorporation of 6-(3-Chloropropanoyl)benzo[d]oxazol-2(3H)-one in synthetic pathways enables the efficient construction of structurally diverse and biologically active molecules.