CAS 40477-61-0: 4-bromo-5-ethylthiophene-2-carboxylic acid

Description: 4-Bromo-5-ethylthiophene-2-carboxylic acid is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. The presence of a bromine atom at the 4-position and an ethylthio group at the 5-position contributes to its unique reactivity and physical properties. The carboxylic acid functional group at the 2-position enhances its acidity and solubility in polar solvents. This compound typically exhibits moderate stability under standard conditions but may be sensitive to strong bases or oxidizing agents. Its molecular structure allows for potential applications in organic synthesis, particularly in the development of pharmaceuticals or agrochemicals. The compound's reactivity can be influenced by the electron-withdrawing effects of the bromine and carboxylic acid groups, making it a valuable intermediate in various chemical reactions. Additionally, its unique properties may lend themselves to applications in materials science, particularly in the development of conductive polymers or organic electronic devices.

Formula: C₇H₇BrO₂S

InChI: InChI=1/C7H7BrO2S/c1-2-5-4(8)3-6(11-5)7(9)10/h3H,2H2,1H3,(H,9,10)

Synonyms:

• 2-Thiophenecarboxylic acid, 4-bromo-5-ethyl-

4-Bromo-5-ethyl-thiophene-2-carboxylic acid

CAS: 40477-61-0

• Purity: 90.0%
• Color and Shape: Solid
• Molecular weight: 235.10000610351562

4-Bromo-5-ethylthiophene-2-carboxylic acid

CAS: 40477-61-0

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• Formula: C₇H₇BrO₂S
• Purity: Min. 95%
• Molecular weight: 235.1 g/mol