1. Home
  2. 3-(4-Hydroxyphenyl)-5-methylisoxazole-4-carboxylic Acid

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

3-(4-Hydroxyphenyl)-5-methylisoxazole-4-carboxylic Acid

Oc1ccc(cc1)c1noc(c1C(=O)O)C Request for Quotation
Chemical Name: 3-(4-Hydroxyphenyl)-5-methylisoxazole-4-carboxylic Acid
CAS Number: 92286-62-9
Product Number: AG003I4I(AGN-PC-0WAFRX)
Synonyms:
MDL No:
Molecular Formula: C11H9NO4
Molecular Weight: 219.1935

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


3-(4-Hydroxyphenyl)-5-methylisoxazole-4-carboxylic acid is a versatile compound utilized in chemical synthesis for its ability to act as a key building block in the creation of various pharmaceuticals, agrochemicals, and functional materials. In organic synthesis, this molecule serves as a crucial intermediate in the preparation of bioactive compounds due to its unique structural features and reactivity.One common application of 3-(4-Hydroxyphenyl)-5-methylisoxazole-4-carboxylic acid is its incorporation into heterocyclic scaffolds, allowing for the development of novel drug candidates with potential therapeutic properties. By functionalizing the carboxylic acid group, chemists can further modify and tailor the compound's pharmacological profile to target specific biological pathways or molecular targets.Additionally, this compound can participate in various organic reactions such as esterification, amidation, and Suzuki coupling, enabling the introduction of diverse functional groups onto the isoxazole core. Its presence in the synthetic route provides opportunities for structural diversification and fine-tuning of properties crucial for bioactivity optimization.Overall, the strategic utilization of 3-(4-Hydroxyphenyl)-5-methylisoxazole-4-carboxylic acid in chemical synthesis allows for the efficient construction of complex molecules with potential applications in drug discovery and material science.