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CAS 338998-93-9

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2-Methylfurane-5-boronic acid pinacol ester

Description:
2-Methylfurane-5-boronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group and a furan ring. This compound typically exhibits a molecular structure that includes a furan moiety substituted with a methyl group and a boronic ester derived from pinacol. The boronic acid functionality is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and materials science. The pinacol ester form enhances the stability and solubility of the boronic acid, facilitating its use in cross-coupling reactions, such as Suzuki reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the compound may exhibit moderate polarity due to the presence of the furan ring and boronic acid group, influencing its reactivity and interaction with other chemical species. Overall, 2-Methylfurane-5-boronic acid pinacol ester is a valuable intermediate in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C11H17BO3
InChI:InChI=1/C11H17BO3/c1-8-6-7-9(13-8)12-14-10(2,3)11(4,5)15-12/h6-7H,1-5H3
SMILES:Cc1ccc(B2OC(C)(C)C(C)(C)O2)o1
Synonyms:
  • 5-Methylfuran-2-boronic acid pinacol ester
  • 4,4,5,5-Tetramethyl-2-(5-Methylfuran-2-Yl)-1,3,2-Dioxaborolane
  • 2-Methylfurane-5-boronic acid pinacol ester
  • 2-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)furan
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(5-methyl-2-furanyl)-
  • 2-(5-Methyl-2-furanyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 5-Methyl-2-furanboronic acid pinacol ester
  • 5-Methyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxoborolan-2-yl)furan, 2-(5-Methylfur-2-yl)-4,4,5
  • 5-Methylfuran-2-boronic acid pinacol ester 95%
  • (5-Methylfuran-2-yl)boronic Acid Pinacol Ester
  • See more synonyms
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