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CAS 936902-06-6

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B-(7-Chlorobenzo[b]thien-2-yl)boronic acid

Description:
B-(7-Chlorobenzo[b]thien-2-yl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a chlorinated benzo[b]thienyl moiety. 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 presence of the chlorine atom on the benzo[b]thienyl ring can influence its reactivity and solubility, potentially enhancing its biological activity or selectivity in chemical reactions. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds in organic synthesis. The compound may also exhibit specific spectral characteristics in techniques such as NMR and IR spectroscopy, which can be utilized for its identification and characterization. Overall, B-(7-Chlorobenzo[b]thien-2-yl)boronic acid represents a versatile building block in the development of pharmaceuticals and agrochemicals.
Formula:C8H6BClO2S
InChI:InChI=1S/C8H6BClO2S/c10-6-3-1-2-5-4-7(9(11)12)13-8(5)6/h1-4,11-12H
InChI key:InChIKey=MCBCDJNNKDMHKL-UHFFFAOYSA-N
SMILES:ClC1=C2C(C=C(B(O)O)S2)=CC=C1
Synonyms:
  • (7-Chloro-1-benzothiophen-2-yl)boronic acid
  • B-(7-Chlorobenzo[b]thien-2-yl)boronic acid
  • Boronic acid, B-(7-chlorobenzo[b]thien-2-yl)-
  • (7-Chlorobenzo[b]thiophen-2-yl)boronic acid
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