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CAS 199659-23-9

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5-CHLOROTHIOPHENE-3-BORONIC ACID

Description:
5-Chlorothiophene-3-boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a thiophene ring that is substituted with a chlorine atom. This compound typically exhibits a planar structure due to the aromatic nature of the thiophene ring, which enhances its stability and reactivity. The boronic acid group (-B(OH)2) is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The chlorine substituent at the 5-position of the thiophene ring can influence the electronic properties and reactivity of the compound, potentially enhancing its role in cross-coupling reactions, such as Suzuki-Miyaura coupling. Additionally, 5-chlorothiophene-3-boronic acid may exhibit solubility in polar organic solvents, which is advantageous for its use in chemical reactions. Overall, this compound serves as a valuable building block in the synthesis of more complex organic molecules and materials.
Formula:C4H4BClO2S
InChI:InChI=1/C4H4BClO2S/c6-4-1-3(2-9-4)5(7)8/h1-2,7-8H
SMILES:c1c(csc1Cl)B(O)O
Synonyms:
  • Akos Brn-1127
  • (5-Chlorothiophen-3-Yl)Boronic Acid
  • 5-CHLOROTHIOPHENE-3-BORONIC ACID
  • Boronic acid, (5-chloro-3-thienyl)- (9CI)
  • 5-chlorothiophen-3-yl-3-boronic acid
  • Boronic acid, B-(5-chloro-3-thienyl)-
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