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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-bromo-1,3-oxazole-2-carboxylic acid

OC(=O)c1nc(co1)Br Request for Quotation
Chemical Name: 4-bromo-1,3-oxazole-2-carboxylic acid
CAS Number: 944906-74-5
Product Number: AG01DMR1(AGN-PC-0ALPYV)
Synonyms:
MDL No:
Molecular Formula: C4H2BrNO3
Molecular Weight: 191.96758

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Chemical Structure


4-Bromo-2-oxazolecarboxylic acid is a valuable building block in chemical synthesis, used for its versatile reactivity in a variety of transformations. This compound serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and functional materials due to its unique structural features and functional groups. In organic synthesis, 4-Bromo-2-oxazolecarboxylic acid can participate in a range of reactions such as nucleophilic substitutions, transition metal-catalyzed cross-coupling reactions, and heterocycle formation. Its incorporation into complex molecules allows for the modulation of biological activity, enhancement of physicochemical properties, and structural diversification. Additionally, the presence of the bromo and oxazole moieties provides opportunities for further derivatization and modification to tailor the compound for specific applications. This compound's significance lies in its ability to enable the efficient construction of diverse chemical structures with potential utility in various fields of research and industry.