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CAS 476004-80-5

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5-Methylthiophene-2-boronic acid pinacol cyclic ester

Description:
5-Methylthiophene-2-boronic acid pinacol cyclic ester is an organoboron compound characterized by the presence of a boronic acid functional group and a thiophene ring. This compound typically exhibits properties associated with boron-containing compounds, such as the ability to form stable complexes with various substrates, making it useful in organic synthesis and medicinal chemistry. The cyclic ester structure contributes to its stability and solubility in organic solvents. The methyl group on the thiophene ring can influence its electronic properties and reactivity, potentially enhancing its utility in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a key method for forming carbon-carbon bonds. Additionally, the presence of the boronic acid moiety allows for further functionalization, making it a versatile intermediate in the synthesis of more complex organic molecules. Overall, this compound is significant in the field of synthetic organic chemistry due to its reactivity and the role it plays in various chemical transformations.
Formula:C11H17BO2S
InChI:InChI=1/C11H17BO2S/c1-8-6-7-9(15-8)12-13-10(2,3)11(4,5)14-12/h6-7H,1-5H3
SMILES:Cc1ccc(B2OC(C)(C)C(C)(C)O2)s1
Synonyms:
  • 4,4,5,5-Tetramethyl-2-(5-Methylthiophen-2-Yl)-1,3,2-Dioxaborolane
  • 5-Methylthiophene-2-boronic acid pinacol ester 95%
  • 4,4,5,5-Tetramethyl-2-(5-methylthiophen-2-yl)
  • 5-Methylthiophene-2-boronic acid pinacol ester, 95%
  • 4,4,5,5-Tetramethyl-2-(5-methyl-2-thienyl)-1,3,2-dioxaborolane
  • 3-hydroxy-2,3-dimethylbutan-2-yl hydrogen (5-methylthiophen-2-yl)boronate
  • 2-(5-Methyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(5-methyl-2-thienyl)-
  • 5-Methylthiophen-2-boronic acid pinacol ester
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