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CAS 177734-82-6

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B-(2-Chloro-3-thienyl)boronic acid

Description:
B-(2-Chloro-3-thienyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group and a thienyl ring substituted with a chlorine atom. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The thienyl moiety contributes to its aromatic character and may influence its reactivity and solubility. B-(2-Chloro-3-thienyl)boronic acid is often utilized in cross-coupling reactions, particularly in the Suzuki-Miyaura reaction, which is a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, the presence of the chlorine atom can enhance the electrophilicity of the compound, potentially affecting its reactivity in various chemical transformations. Overall, this compound is valuable in the development of pharmaceuticals and agrochemicals, as well as in materials science.
Formula:C4H4BClO2S
InChI:InChI=1S/C4H4BClO2S/c6-4-3(5(7)8)1-2-9-4/h1-2,7-8H
InChI key:InChIKey=JWVLMZZYJOJCTI-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)SC=C1
Synonyms:
  • (2-Chloro-3-thienyl)boronic acid
  • (2-Chlorothien-3-yl)boronic acid
  • (2-Chlorothiophen-3-yl)boronic acid
  • (2-Chlorothiophen-3-yl)dihydroxyborane
  • 2-Chloothiophene-3-Boronic Acid
  • 2-Chloro-3-thiopheneboronic acid
  • 2-Chlorothiophen-3-Boronic Acid
  • 2-Chlorothiophen-3-Ylboronic Acid
  • 2-Chlorothiophen-3-Ylboronic Acid ,97%
  • 2-Chlorothiophene-3-Boronic
  • See more synonyms
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