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CAS 1256355-67-5

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B-[2-[(3-Cyanophenyl)methoxy]phenyl]boronic acid

Description:
B-[2-[(3-Cyanophenyl)methoxy]phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications such as organic synthesis and medicinal chemistry. The compound features a biphenyl structure with a methoxy group and a cyano-substituted phenyl moiety, contributing to its unique electronic properties and potential reactivity. The presence of the boronic acid group allows for participation in Suzuki coupling reactions, a widely used method for forming carbon-carbon bonds. Additionally, the cyano group may enhance the compound's polarity and solubility in polar solvents, influencing its behavior in biological systems. Overall, this compound's structural characteristics suggest potential utility in drug development and materials science, particularly in the design of sensors or catalysts. As with many boronic acids, it is important to handle this compound with care due to its reactivity and potential environmental impact.
Formula:C14H12BNO3
InChI:InChI=1S/C14H12BNO3/c16-9-11-4-3-5-12(8-11)10-19-14-7-2-1-6-13(14)15(17)18/h1-8,17-18H,10H2
InChI key:InChIKey=GLFQWDKMRRYVDL-UHFFFAOYSA-N
SMILES:O(CC1=CC(C#N)=CC=C1)C2=C(B(O)O)C=CC=C2
Synonyms:
  • B-[2-[(3-Cyanophenyl)methoxy]phenyl]boronic acid
  • Boronic acid, B-[2-[(3-cyanophenyl)methoxy]phenyl]-
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