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CAS 69399-79-7

:

3-(2-Chloro-6-fluorophenyl)-5-methylisoxazole-4-carbonyl chloride

Description:
3-(2-Chloro-6-fluorophenyl)-5-methylisoxazole-4-carbonyl chloride 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 a carbonyl chloride functional group, making it a reactive acyl chloride, which is typically used in organic synthesis for acylation reactions. The presence of the 2-chloro-6-fluorophenyl group contributes to its potential biological activity and lipophilicity, while the methyl group at the 5-position of the isoxazole ring can influence its electronic properties and steric hindrance. The compound is likely to be a solid at room temperature and may exhibit moderate to high solubility in organic solvents. Due to the presence of chlorine and fluorine substituents, it may also display unique reactivity patterns and stability characteristics. As with many acyl chlorides, it is important to handle this compound with care, as it can be corrosive and may react violently with water, releasing hydrochloric acid.
Formula:C11H6Cl2FNO2
InChI:InChI=1/C11H6Cl2FNO2/c1-5-8(11(13)16)10(15-17-5)9-6(12)3-2-4-7(9)14/h2-4H,1H3
InChI key:InChIKey=XJCUKCOLGJDGGN-UHFFFAOYSA-N
SMILES:ClC1=C(C(F)=CC=C1)C=2C(C(Cl)=O)=C(C)ON2
Synonyms:
  • 3-(2-Chloro-6-Fluorophenyl)-5-Methylis
  • 3-(2-Chloro-6-fluorophenyl)-5-methyl-4-isoxazolecarbonyl chloride
  • 3-(2-Chloro-6-fluorophenyl)-5-methylisoxazol-4-oyl chloride
  • 3-(2-Chloro-6-fluorophenyl)-5-methylisoxazole-4-carbonyl chloride
  • 3-(2-Chloro-6-fluorophenyl)-5-methylisoxazole-4-carbonylchloride
  • 3-(6-Fluoro-2-chlorophenyl)-5-methylisoxazol-4-carbonyl chloride
  • 4-(Chlorocarbonyl)-3-(2-Chloro-6-fluorophenyl)-5-methylisoxazole
  • 4-Isoxazolecarbonyl chloride, 3-(2-chloro-6-fluorophenyl)-5-methyl-
  • FCMIC Chloride
  • 3-(2-Chloro-6-fluorophenyl)-5-methylisoxazole-4-carbonyl chloride 97%
  • See more synonyms
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