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CAS 33282-23-4

:

5-(4-bromophenyl)isoxazole-3-carboxylic acid

Description:
5-(4-Bromophenyl)isoxazole-3-carboxylic acid is an organic compound characterized by its isoxazole ring, which is a five-membered heterocyclic structure containing both nitrogen and oxygen atoms. The presence of the 4-bromophenyl group indicates that a bromine atom is substituted on the phenyl ring at the para position, contributing to the compound's unique chemical properties and potential reactivity. The carboxylic acid functional group (-COOH) at the 3-position of the isoxazole ring imparts acidic characteristics, making it capable of participating in various chemical reactions, such as esterification or amidation. This compound may exhibit biological activity, making it of interest in pharmaceutical research. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of new therapeutic agents. Additionally, the presence of bromine can enhance lipophilicity and influence the compound's interaction with biological targets. Overall, 5-(4-bromophenyl)isoxazole-3-carboxylic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C10H6BrNO3
InChI:InChI=1/C10H6BrNO3/c11-7-3-1-6(2-4-7)9-5-8(10(13)14)12-15-9/h1-5H,(H,13,14)
SMILES:c1cc(ccc1c1cc(C(=O)O)no1)Br
Synonyms:
  • 33282-23-4
  • 5-(4-Bro?mophenyl)-3-isoxazo?lecarboxy?lic acid
  • 5-(4-Bromophenyl)-1,2-oxazole-3-carboxylic acid
  • T5Noj Cr De& Evq
  • 5-(4-Bromophenyl)isoxazole-3-carboxylic acid
  • 5-(4-BROMOPHENYL)ISOXAZOLE-3-CARBOXYLIC&
  • 3-Isoxazolecarboxylic acid, 5-(4-bromophenyl)-
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