CAS 869496-62-8
:3-(3-Bromophenyl)-5-isoxazolecarboxaldehyde
Description:
3-(3-Bromophenyl)-5-isoxazolecarboxaldehyde is a chemical compound characterized by its unique isoxazole ring structure, which contributes to its reactivity and potential applications in organic synthesis and medicinal chemistry. The presence of a bromophenyl group enhances its electrophilic properties, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. The aldehyde functional group (-CHO) at the isoxazole's 5-position is significant for its reactivity, allowing for further derivatization and functionalization. This compound may exhibit biological activity, making it of interest in pharmaceutical research, particularly in the development of new therapeutic agents. Its molecular structure suggests potential interactions with biological targets, which can be explored through structure-activity relationship studies. Additionally, the compound's solubility and stability in various solvents can influence its practical applications in laboratory settings. Overall, 3-(3-Bromophenyl)-5-isoxazolecarboxaldehyde is a versatile compound with promising implications in both synthetic and medicinal chemistry.
Formula:C10H6BrNO2
InChI:InChI=1S/C10H6BrNO2/c11-8-3-1-2-7(4-8)10-5-9(6-13)14-12-10/h1-6H
InChI key:InChIKey=IJRDQYJFADPHNO-UHFFFAOYSA-N
SMILES:C(=O)C1=CC(=NO1)C2=CC(Br)=CC=C2
Synonyms:- 3-(3-Bromo-Phenyl)-Isoxazole-5-Carbaldehyde
- 3-(3-Bromophenyl)-5-isoxazolecarboxaldehyde
- 5-Isoxazolecarboxaldehyde, 3-(3-bromophenyl)-
Sort by
The purity filter is not visible because current products do not have associated purity data for filtering.
Found 1 products.
