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CAS 1217501-16-0

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B-(5-Bromo-4-methyl-2-thienyl)boronic acid

Description:
B-(5-Bromo-4-methyl-2-thienyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a thienyl ring that is substituted with a bromine atom and a methyl group. This compound typically exhibits properties such as moderate solubility in polar organic solvents and can participate in various chemical reactions, including Suzuki coupling, which is significant in organic synthesis for forming carbon-carbon bonds. The presence of the bromine atom enhances its reactivity, making it a useful intermediate in the synthesis of more complex organic molecules. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications and drug delivery systems. The compound's structure suggests potential applications in medicinal chemistry and materials science, particularly in the development of organic semiconductors or as a building block in the synthesis of biologically active compounds. Overall, B-(5-Bromo-4-methyl-2-thienyl)boronic acid is a versatile compound with significant implications in synthetic organic chemistry.
Formula:C5H6BBrO2S
InChI:InChI=1S/C5H6BBrO2S/c1-3-2-4(6(8)9)10-5(3)7/h2,8-9H,1H3
InChI key:InChIKey=UOYBEXPZKLEGAF-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(C)=C(Br)S1
Synonyms:
  • B-(5-Bromo-4-methyl-2-thienyl)boronic acid
  • Boronic acid, B-(5-bromo-4-methyl-2-thienyl)-
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