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CAS 221061-14-9

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2-bromo-5-methylthiophene-3-carboxylic acid

Description:
2-Bromo-5-methylthiophene-3-carboxylic acid is an organic compound characterized by its thiophene ring structure, which includes a bromine substituent and a carboxylic acid functional group. The presence of the bromine atom at the 2-position and a methylthio group at the 5-position contributes to its unique reactivity and properties. This compound is typically a solid at room temperature and is soluble in polar organic solvents due to the carboxylic acid group, which can engage in hydrogen bonding. The thiophene ring imparts aromatic characteristics, making it relatively stable and resistant to oxidation. Its carboxylic acid functionality allows for potential applications in organic synthesis, particularly in the formation of esters or amides. Additionally, the compound may exhibit biological activity, making it of interest in pharmaceutical research. Overall, 2-bromo-5-methylthiophene-3-carboxylic acid is a versatile building block in organic chemistry with potential applications in various fields.
Formula:C6H5BrO2S
InChI:InChI=1/C6H5BrO2S/c1-3-2-4(6(8)9)5(7)10-3/h2H,1H3,(H,8,9)
SMILES:Cc1cc(c(Br)s1)C(=O)O
Synonyms:
  • 3-Thiophenecarboxylic acid, 2-bromo-5-methyl-
  • 2-Bromo-5-methylthiophene-3-carboxylic acid
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