CAS 1188228-73-0

5-Chloro-3-(4-fluorophenyl)-4-isoxazolecarboxaldehyde

Description:

5-Chloro-3-(4-fluorophenyl)-4-isoxazolecarboxaldehyde is a chemical compound characterized by its isoxazole ring, which is a five-membered heterocyclic structure containing both nitrogen and oxygen atoms. This compound features a chloro substituent at the 5-position and a 4-fluorophenyl group at the 3-position of the isoxazole ring, contributing to its unique reactivity and potential biological activity. The presence of the aldehyde functional group at the 4-position enhances its reactivity, making it a valuable intermediate in organic synthesis and medicinal chemistry. The compound's molecular structure suggests potential applications in pharmaceuticals, particularly in the development of compounds with antimicrobial or anti-inflammatory properties. Its specific interactions and behavior in biological systems would depend on various factors, including its solubility, stability, and the presence of other functional groups. As with many synthetic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.

Formula: C₁₀H₅ClFNO₂

InChI: InChI=1S/C10H5ClFNO2/c11-10-8(5-14)9(13-15-10)6-1-3-7(12)4-2-6/h1-5H

InChI key: InChIKey=LBUHJDJXBDRJAW-UHFFFAOYSA-N

SMILES: C(=O)C=1C(=NOC1Cl)C2=CC=C(F)C=C2

Synonyms:

• 4-Isoxazolecarboxaldehyde, 5-chloro-3-(4-fluorophenyl)-
• 5-Chloro-3-(4-fluorophenyl)-4-isoxazolecarboxaldehyde

5-chloro-3-(4-fluorophenyl)-1,2-oxazole-4-carbaldehyde

CAS: 1188228-73-0

Formula: C₁₀H₅ClFNO₂

Purity: 95.0%

Molecular weight: 225.6

Ref: 10-F522270