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CAS 25629-50-9

:

3-(2-Chlorophenyl)-5-methylisoxazole-4-carbonyl chloride

Description:
3-(2-Chlorophenyl)-5-methylisoxazole-4-carbonyl chloride, with the CAS number 25629-50-9, is a chemical compound characterized by its isoxazole ring structure, which is a five-membered heterocyclic compound containing both nitrogen and oxygen atoms. This compound features a chlorophenyl group, which contributes to its potential reactivity and biological activity. The carbonyl chloride functional group indicates that it is an acyl chloride, making it reactive towards nucleophiles, which is useful in various synthetic applications. The presence of the methyl group on the isoxazole ring can influence its solubility and reactivity. This compound may be utilized in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals, due to its ability to participate in acylation reactions. As with many chlorinated compounds, it may exhibit specific environmental and health considerations, necessitating careful handling and disposal. Overall, its unique structure and functional groups make it a valuable intermediate in chemical synthesis.
Formula:C11H7Cl2NO2
InChI:InChI=1S/C11H7Cl2NO2/c1-6-9(11(13)15)10(14-16-6)7-4-2-3-5-8(7)12/h2-5H,1H3
InChI key:InChIKey=BPDBLWKFVXHGFT-UHFFFAOYSA-N
SMILES:C(Cl)(=O)C=1C(=NOC1C)C2=C(Cl)C=CC=C2
Synonyms:
  • 3-(2-Chlorophenyl)-5-methyl-1,2-oxazole-4-carbonyl chloride
  • 3-(2-Chlorophenyl)-5-methyl-4-isoxazolecarbonyl chloride
  • 3-(2-Chlorophenyl)-5-methylisoxazol-4-carbonyl chloride
  • 3-(o-Chlorophenyl)-5-methyl-4-isoxazolecarbonyl chloride
  • 4-Isoxazolecarbonyl chloride, 3-(2-chlorophenyl)-5-methyl-
  • 4-Isoxazolecarbonyl chloride, 3-(o-chlorophenyl)-5-methyl-
  • CMIC Chloride
  • NSC 81237
  • 3-(2-Chlorophenyl)-5-methylisoxazole-4-carbonyl chloride
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