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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-(2-methoxyphenyl)-5-methyl-

COc1ccccc1c1noc(c1C(=O)O)C Request for Quotation
Chemical Name: 4-Isoxazolecarboxylic acid, 3-(2-methoxyphenyl)-5-methyl-
CAS Number: 93041-44-2
Product Number: AG00GTM8(AGN-PC-0LU59F)
Synonyms:
MDL No:
Molecular Formula: C12H11NO4
Molecular Weight: 233.2200

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(2-Methoxyphenyl)-5-methylisoxazole-4-carboxylic acid is a versatile compound commonly utilized in chemical synthesis for various applications. In organic chemistry, this compound serves as a key building block for the synthesis of more complex molecules due to its unique structural properties. Specifically, its isoxazole ring structure and carboxylic acid functionality enable it to participate in diverse chemical reactions, including condensation, esterification, and decarboxylation reactions, resulting in the formation of new compounds with altered physicochemical properties. Additionally, the presence of the methoxy and methyl substituents on the phenyl and isoxazole rings, respectively, provides opportunities for further functionalization through selective derivatization reactions, allowing for the tailored design of novel organic molecules with specific properties and functionalities. Overall, the application of 3-(2-Methoxyphenyl)-5-methylisoxazole-4-carboxylic acid in chemical synthesis contributes to the advancement of organic chemistry by facilitating the efficient and strategic construction of diverse molecular architectures for various industrial and research purposes.