CAS 53983-15-6
:ethyl 5-amino-4-phenylisoxazole-3-carboxylate
Description:
Ethyl 5-amino-4-phenylisoxazole-3-carboxylate is a chemical compound characterized by its isoxazole ring structure, which is a five-membered heterocyclic compound containing both nitrogen and oxygen. This substance features an ethyl ester functional group, contributing to its solubility and reactivity. The presence of an amino group at the 5-position and a phenyl group at the 4-position of the isoxazole ring enhances its potential for biological activity, making it of interest in medicinal chemistry. The carboxylate group at the 3-position further adds to its chemical reactivity, allowing for various derivatization reactions. Ethyl 5-amino-4-phenylisoxazole-3-carboxylate may exhibit properties such as moderate polarity and potential interactions with biological targets, which could be explored for therapeutic applications. Its CAS number, 53983-15-6, allows for easy identification in chemical databases and literature. Overall, this compound represents a versatile scaffold for further chemical modifications and investigations in drug development.
Formula:C12H12N2O3
InChI:InChI=1/C12H12N2O3/c1-2-16-12(15)10-9(11(13)17-14-10)8-6-4-3-5-7-8/h3-7H,2,13H2,1H3
SMILES:CCOC(=O)c1c(c2ccccc2)c(N)on1
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
Ethyl 5-amino-4-phenylisoxazole-3-carboxylate
CAS:Formula:C12H12N2O3Purity:97%Color and Shape:SolidMolecular weight:232.2353Ethyl 5-amino-4-phenylisoxazole-3-carboxylate
CAS:Ethyl 5-amino-4-phenylisoxazole-3-carboxylatePurity:97%Molecular weight:232.24g/molethyl 5-amino-4-phenyl-1,2-oxazole-3-carboxylate
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H12N2O3Purity:Min. 95%Molecular weight:232.2 g/mol




