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CAS 871332-95-5

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4-Chloro-3-cyanophenylboronic acid

Description:
4-Chloro-3-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. This compound features a chloro substituent and a cyano group on a phenyl ring, contributing to its reactivity and potential applications in cross-coupling reactions, such as Suzuki-Miyaura coupling. The presence of the cyano group enhances its electronic properties, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, the boronic acid moiety allows for the formation of boronate esters, which are important in the development of sensors and in the field of materials science. The compound is typically handled with care due to its potential reactivity and should be stored under appropriate conditions to maintain stability. Overall, 4-Chloro-3-cyanophenylboronic acid is a versatile building block in synthetic organic chemistry.
Formula:C7H5BClNO2
InChI:InChI=1/C7H5BClNO2/c9-7-2-1-6(8(11)12)3-5(7)4-10/h1-3,11-12H
SMILES:c1cc(c(cc1B(O)O)C#N)Cl
Synonyms:
  • 4-Chloro-3-cyanobenzeneboronic acid
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