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CAS 4402-83-9

:

methyl 3-(2,6-dichlorophenyl)-5-methylisoxazole-4-carboxylate

Description:
Methyl 3-(2,6-dichlorophenyl)-5-methylisoxazole-4-carboxylate, with the CAS number 4402-83-9, is a chemical compound characterized by its isoxazole structure, which features a five-membered ring containing both nitrogen and oxygen atoms. This compound exhibits a carboxylate functional group, contributing to its potential reactivity and solubility properties. The presence of the 2,6-dichlorophenyl group enhances its lipophilicity and may influence its biological activity, making it of interest in pharmaceutical research. Methyl esters, like this compound, are often used in organic synthesis and can serve as intermediates in the production of various chemical entities. The compound's molecular structure suggests it may exhibit specific interactions with biological targets, which could be explored for therapeutic applications. Additionally, its stability and reactivity can be influenced by the substituents on the isoxazole ring and the phenyl group, making it a subject of interest in medicinal chemistry and agrochemical research.
Formula:C12H9Cl2NO3
InChI:InChI=1/C12H9Cl2NO3/c1-6-9(12(16)17-2)11(15-18-6)10-7(13)4-3-5-8(10)14/h3-5H,1-2H3
SMILES:Cc1c(c(c2c(cccc2Cl)Cl)no1)C(=O)OC
Synonyms:
  • Methyl 3-(2,6-Dichlorophenyl)-5-Methyl-1,2-Oxazole-4-Carboxylate
  • 4-Isoxazolecarboxylic acid, 3-(2,6-dichlorophenyl)-5-methyl-, methyl ester
  • BUTTPARK 91\12-14
  • METHYL 3-(2,6-DICHLOROPHENYL)-5-METHYLISOXAZOLE-4-CARBOXYLATE
  • METHYL 3-(2,6-DICHLOROPHENYL)-5-METHYL-4-ISOXAZOLECARBOXYLATE
  • SALOR-INT L322032-1EA
  • 3-(2,6-Dichlorophenyl)-5-Methyl-4-isoxazolylcarboxylic Acid Methyl Ester
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