3-(4-Fluorophenyl)-5-methyl-4-isoxazolecarbonyl chloride, with the CAS number 465514-05-0, is a chemical compound characterized by its isoxazole ring structure, which is a five-membered heterocyclic compound containing both nitrogen and oxygen. This compound features a carbonyl chloride functional group, indicating it is a reactive acyl chloride, which can participate in various chemical reactions, such as acylation. The presence of a 4-fluorophenyl group suggests that it may exhibit unique electronic properties due to the electronegative fluorine atom, potentially influencing its reactivity and interactions with biological targets. Additionally, the methyl group at the 5-position of the isoxazole ring may affect the steric and electronic characteristics of the molecule. This compound is likely to be of interest in medicinal chemistry and material science due to its potential applications in drug development and synthesis of novel compounds. As with many acyl chlorides, it should be handled with care due to its reactivity and potential hazards associated with its use.

3-(4-fluorophenyl)-5-methyl-4-isoxazolecarbonyl chloride

465514-05-0: 3-(4-Fluorophenyl)-5-methyl-4-isoxazolecarbonyl chloride, with the CAS number 465514-05-0, is a chemical compound characterized by its isoxazole ring structure, which is a five-membered heterocyclic compound containing both nitrogen and oxygen. This compound features a carbonyl chloride functional group, indicating it is a reactive acyl chloride, which can participate in various chemical reactions, such as acylation. The presence of a 4-fluorophenyl group suggests that it may exhibit unique electronic properties due to the electronegative fluorine atom, potentially influencing its reactivity and interactions with biological targets. Additionally, the methyl group at the 5-position of the isoxazole ring may affect the steric and electronic characteristics of the molecule. This compound is likely to be of interest in medicinal chemistry and material science due to its potential applications in drug development and synthesis of novel compounds. As with many acyl chlorides, it should be handled with care due to its reactivity and potential hazards associated with its use.

3-(4-Fluorophenyl)-5-methylisoxazole-4-carbonyl chloride

CAS 465514-05-0

3-(4-fluorophenyl)-5-methyl-4-isoxazolecarbonyl chloride

3-(4-Fluorophenyl)-5-methylisoxazole-4-carbonyl chloride

Ref: 54-PC31883