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CAS 49615-71-6

:

4-(4-Bromophenyl)-1,2,5-oxadiazol-3-amine

Description:
4-(4-Bromophenyl)-1,2,5-oxadiazol-3-amine is a chemical compound characterized by its oxadiazole ring, which is a five-membered heterocyclic structure containing two nitrogen atoms and three carbon atoms. The presence of a bromophenyl group indicates that a bromine atom is substituted on a phenyl ring, contributing to the compound's unique reactivity and potential biological activity. This compound typically exhibits properties such as moderate solubility in organic solvents and may have specific interactions with biological targets due to the amine functional group. The oxadiazole moiety is known for its applications in pharmaceuticals and materials science, often serving as a scaffold for drug development. Additionally, the bromine substituent can enhance the compound's lipophilicity and influence its electronic properties, making it a candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. Overall, 4-(4-Bromophenyl)-1,2,5-oxadiazol-3-amine is of interest in both synthetic chemistry and medicinal chemistry due to its structural features and potential applications.
Formula:C8H6BrN3O
InChI:InChI=1S/C8H6BrN3O/c9-6-3-1-5(2-4-6)7-8(10)12-13-11-7/h1-4H,(H2,10,12)
InChI key:InChIKey=QWSVUZLCBMDUQJ-UHFFFAOYSA-N
SMILES:NC=1C(=NON1)C2=CC=C(Br)C=C2
Synonyms:
  • 4-(4-Bromophenyl)-1,2,5-oxadiazol-3-amine
  • 1,2,5-Oxadiazol-3-amine, 4-(4-bromophenyl)-
  • Furazanamine, 4-(4-bromophenyl)-
  • 3-Amino-4-(p-bromophenyl)-1,2,5-oxadiazole
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