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CAS 214360-46-0

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(3-Cyanophenyl)boronic acid pinacol ester

Description:
(3-Cyanophenyl)boronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group and a cyanophenyl moiety. This compound typically exhibits a white to off-white crystalline appearance and is soluble in organic solvents such as dichloromethane and ethanol. The boronic acid functionality allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds in organic synthesis. The presence of the cyano group enhances the compound's reactivity and can influence its electronic properties, making it useful in the development of pharmaceuticals and agrochemicals. Additionally, the pinacol ester moiety provides stability to the boronic acid group, facilitating its handling and storage. Overall, (3-Cyanophenyl)boronic acid pinacol ester is a valuable intermediate in synthetic organic chemistry, particularly in the construction of complex molecular architectures.
Formula:C13H16BNO2
InChI:InChI=1S/C13H16BNO2/c1-12(2)13(3,4)17-14(16-12)11-7-5-6-10(8-11)9-15/h5-8H,1-4H3
InChI key:InChIKey=FIGQEPXOSAFKTA-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(C#N)=CC=C2
Synonyms:
  • (3-Cyanophenyl)boronic acid pinacol ester
  • 1,1,2,2-Tetramethyldimethylene (3-cyanophenyl)boronate
  • 3-Cyanphenylboronic Acid Pinacol Ester
  • Benzonitrile, 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 2-(3-Cyanophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile
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