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CAS 16883-16-2

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5-Methyl-3-phenylisoxazole-4-carbonyl chloride

Description:
5-Methyl-3-phenylisoxazole-4-carbonyl chloride, with the CAS number 16883-16-2, 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 carbonyl chloride functional group, making it a reactive acyl chloride. The presence of the methyl and phenyl substituents on the isoxazole ring contributes to its unique chemical properties, influencing its reactivity and potential applications in organic synthesis. Typically, compounds like this are utilized in the synthesis of pharmaceuticals and agrochemicals due to their ability to participate in various chemical reactions, such as acylation and nucleophilic substitution. The carbonyl chloride group is particularly significant as it can react with nucleophiles, facilitating the formation of amides or esters. As with many chlorinated compounds, appropriate safety measures should be taken when handling this substance, as it may pose hazards such as irritancy or reactivity with moisture.
Formula:C11H8ClNO2
InChI:InChI=1/C11H8ClNO2/c1-7-9(11(12)14)10(13-15-7)8-5-3-2-4-6-8/h2-6H,1H3
InChI key:InChIKey=HXEVQMXCHCDPSO-UHFFFAOYSA-N
SMILES:C(Cl)(=O)C=1C(=NOC1C)C2=CC=CC=C2
Synonyms:
  • 3-Phenyl-5-methyl-4-isoxazolecarbonyl chloride
  • 3-Phenyl-5-methylisoxazol-4-carboxyl chloride
  • 4-Isoxazolecarbonyl chloride, 5-methyl-3-phenyl-
  • 5-Methyl-3-phenyl-1,2-oxazole-4-carbonyl chloride
  • 5-Methyl-3-phenyl-4-isoxazolecarbonyl chloride
  • 5-Methyl-3-phenyl-4-isoxazolylcarbonyl chloride
  • PMIC Chloride
  • 5-Methyl-3-phenylisoxazole-4-carbonyl chloride
  • 5-Methyl-3-phenylisoxazole-4-carboxylic acid chloride
  • 5-Methyl-3-phenyl-4-isoxazolecarbonylchloride
  • See more synonyms
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