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CAS 870238-36-1

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5-Chloro-2-formylphenylboronic acid

Description:
5-Chloro-2-formylphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group and a chloro-substituted aromatic ring. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the boronic acid moiety. The presence of the formyl group (-CHO) enhances its reactivity, making it useful in various organic synthesis applications, particularly in the formation of carbon-carbon bonds through Suzuki coupling reactions. The chloro substituent can also participate in nucleophilic substitution reactions, further expanding its utility in synthetic chemistry. 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. Safety considerations should be taken into account when handling this compound, as boronic acids can be irritants and may pose environmental hazards. Overall, 5-Chloro-2-formylphenylboronic acid is a versatile building block in organic synthesis and medicinal chemistry.
Formula:C7H6BClO3
InChI:InChI=1/C7H6BClO3/c9-6-2-1-5(4-10)7(3-6)8(11)12/h1-4,11-12H
SMILES:c1cc(cc(c1C=O)B(O)O)Cl
Synonyms:
  • (5-Chloro-2-formylphenyl)boronic acid
  • 5-Chloro-2-formylphenylboronicacid
  • Boronic acid, B-(5-chloro-2-formylphenyl)-
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