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CAS 915763-60-9

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3-Chloro-5-cyanophenylboronicacid

Description:
3-Chloro-5-cyanophenylboronic 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, particularly in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with both a chlorine atom and a cyano group, which contribute to its reactivity and solubility properties. The chlorine atom can enhance electrophilicity, while the cyano group can serve as a versatile handle for further chemical modifications. This compound is typically used in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds, and is valuable in the development of pharmaceuticals and agrochemicals. Additionally, its boronic acid moiety allows for potential applications in sensor technology and materials science. As with many boronic acids, it is important to handle this compound with care, as it may exhibit sensitivity to moisture and air, which can affect its stability and reactivity.
Formula:C7H5BClNO2
Synonyms:
  • (3-Chloro-5-Cyanophenyl)Boronic Acid
  • 5-Chloro-3-Cyanophenylboronic acid
  • Boronic acid, B-(3-chloro-5-cyanophenyl)-
  • 3-Chloro-5-cyanobenzeneboronic Acid
  • (3-Chloro-5-cyanophenyl)
  • (3-Chloro-5-cyanophenyl)boronic acid 98%
  • 3-Chloro-5-cyanophenylboronic Acid (contains varying amounts of Anhydride)
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