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CAS 352530-25-7

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5-Formyl-4-methylthiophene-2-boronic acid

Description:
5-Formyl-4-methylthiophene-2-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its reactivity in various organic synthesis applications, particularly in Suzuki coupling reactions. This compound features a thiophene ring, which contributes to its aromatic properties and potential electronic characteristics. The formyl group (-CHO) attached to the thiophene enhances its reactivity, making it suitable for further functionalization. The methylthio group (-S-CH3) at the 4-position of the thiophene ring can influence the compound's solubility and electronic properties. Typically, boronic acids are utilized in medicinal chemistry and materials science due to their ability to form stable complexes with diols and their role in the synthesis of complex organic molecules. The compound's structure suggests it may exhibit interesting properties such as fluorescence or conductivity, depending on the specific conditions and substituents involved. Overall, 5-Formyl-4-methylthiophene-2-boronic acid is a versatile building block in organic synthesis and materials development.
Formula:C6H7BO3S
InChI:InChI=1/C6H7BO3S/c1-4-2-6(7(9)10)11-5(4)3-8/h2-3,9-10H,1H3
SMILES:Cc1cc(B(O)O)sc1C=O
Synonyms:
  • (5-Formyl-4-Methyl-2-Thienyl)Boronic Acid
  • 5-Formyl-4-methylthiophene-2-boronic acid, 97%
  • 5-Borono-3-methylthiophene-2-carboxaldehyde
  • 5-formyl-4-methylthiophen-2-ylboronic acid
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