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CAS 1023595-18-7

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

Description:
B-(2-Cyano-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 cyano group. This compound typically exhibits properties such as being a solid at room temperature, with potential solubility in polar organic solvents. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis and materials science. The cyano group contributes to its electronic properties, potentially enhancing reactivity and stability. Additionally, the thienyl ring can impart unique optical and electronic characteristics, which may be useful in applications such as organic electronics or sensors. Overall, B-(2-Cyano-3-thienyl)boronic acid is notable for its versatility in synthetic chemistry and potential applications in advanced materials.
Formula:C5H4BNO2S
InChI:InChI=1S/C5H4BNO2S/c7-3-5-4(6(8)9)1-2-10-5/h1-2,8-9H
InChI key:InChIKey=RFWCHPVGCQCEQB-UHFFFAOYSA-N
SMILES:C(#N)C1=C(B(O)O)C=CS1
Synonyms:
  • (2-Cyanothiophen-3-yl)boronicacid
  • (2-Cyanothiophen-3-yl)boronic acid
  • B-(2-Cyano-3-thienyl)boronic acid
  • Boronic acid, B-(2-cyano-3-thienyl)-
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