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CAS 850568-67-1

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B-[4-(1-Cyano-1-methylethyl)phenyl]boronic acid

Description:
B-[4-(1-Cyano-1-methylethyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a cyano 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 and medicinal chemistry. The cyano group contributes to its electronic properties, potentially enhancing its reactivity and making it useful in the development of pharmaceuticals and agrochemicals. 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 it may have applications in materials science and catalysis, given the versatility of boron in forming diverse coordination complexes. Overall, B-[4-(1-Cyano-1-methylethyl)phenyl]boronic acid is a valuable compound in synthetic organic chemistry with potential applications across various fields.
Formula:C10H12BNO2
InChI:InChI=1S/C10H12BNO2/c1-10(2,7-12)8-3-5-9(6-4-8)11(13)14/h3-6,13-14H,1-2H3
InChI key:InChIKey=BNXBFDTWYHAEIR-UHFFFAOYSA-N
SMILES:C(C#N)(C)(C)C1=CC=C(B(O)O)C=C1
Synonyms:
  • 2-(4-Boronophenyl)-2-methylpropanenitrile
  • 4-(2-Cyanopropan-2-yl)benzeneboronic acid
  • B-[4-(1-Cyano-1-methylethyl)phenyl]boronic acid
  • Boronic acid, [4-(1-cyano-1-methylethyl)phenyl]-
  • [4-(1-Cyano-1-methylethyl)phenyl]boronic acid
  • [4-(2-Cyanopropan-2-Yl)Phenyl]Boronic Acid
  • boronic acid, B-[4-(1-cyano-1-methylethyl)phenyl]-
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