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CAS 89499-51-4

:

Methyl 4-amino-5-bromo-2-thiophenecarboxylate

Description:
Methyl 4-amino-5-bromo-2-thiophenecarboxylate is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features a carboxylate group, an amino group, and a bromine substituent, contributing to its reactivity and potential applications in various chemical reactions. The presence of the amino group suggests that it can participate in nucleophilic substitution reactions, while the bromine atom can serve as a leaving group or participate in cross-coupling reactions. The methyl ester functionality indicates that it can undergo hydrolysis to yield the corresponding carboxylic acid. This compound may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its unique structure allows for potential interactions with biological targets, and it may serve as a building block for synthesizing more complex molecules. As with many organic compounds, proper handling and safety precautions are essential due to potential toxicity or reactivity.
Formula:C6H6BrNO2S
InChI:InChI=1S/C6H6BrNO2S/c1-10-6(9)4-2-3(8)5(7)11-4/h2H,8H2,1H3
InChI key:InChIKey=SLMFLUFQWGQAPZ-UHFFFAOYSA-N
SMILES:C(OC)(=O)C1=CC(N)=C(Br)S1
Synonyms:
  • 2-Thiophenecarboxylic acid, 4-amino-5-bromo-, methyl ester
  • Methyl 4-amino-5-bromo-2-thiophenecarboxylate
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