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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-Isoxazolecarboxylic acid, 3-(4-bromophenyl)-5-methyl-

Brc1ccc(cc1)c1noc(c1C(=O)O)C Request for Quotation
Chemical Name: 4-Isoxazolecarboxylic acid, 3-(4-bromophenyl)-5-methyl-
CAS Number: 91182-58-0
Product Number: AG006Q76(AGN-PC-03NRSO)
Synonyms:
MDL No:
Molecular Formula: C11H8BrNO3
Molecular Weight: 282.0901

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Chemical Structure


3-(4-Bromophenyl)-5-methylisoxazole-4-carboxylic acid is a versatile compound widely utilized in chemical synthesis. With its unique structure and functional groups, this molecule serves as a valuable building block in the creation of various organic compounds.One key application of 3-(4-Bromophenyl)-5-methylisoxazole-4-carboxylic acid is its role as a precursor in the synthesis of pharmaceutical compounds. By incorporating this compound into a synthetic pathway, chemists can introduce specific functionalities and structural motifs necessary for the desired biological activity of the final drug product.Furthermore, this compound can participate in cross-coupling reactions, allowing for the formation of complex molecules through the construction of carbon-carbon or carbon-heteroatom bonds. Its reactive nature enables the efficient synthesis of diverse chemical entities with potential applications in drug discovery, materials science, and agrochemicals.In addition, 3-(4-Bromophenyl)-5-methylisoxazole-4-carboxylic acid can be modified through various functional group transformations, such as esterification, amidation, or halogenation, expanding its synthetic utility and versatility. This flexibility makes it a valuable tool for organic chemists seeking to access novel molecular structures for research and development purposes.