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CAS 870718-05-1

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[3-(Ethylthio)phenyl]boronic acid

Description:
[3-(Ethylthio)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that has an ethylthio substituent at the meta position. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The ethylthio group enhances its solubility in organic solvents and may influence its reactivity and interaction with biological targets. The compound is generally stable under standard conditions but may undergo hydrolysis in the presence of moisture, leading to the formation of boronic acid derivatives. Its reactivity can be exploited in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a key method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Overall, [3-(Ethylthio)phenyl]boronic acid is a versatile building block in synthetic chemistry, particularly in the development of pharmaceuticals and agrochemicals.
Formula:C8H11BO2S
InChI:InChI=1S/C8H11BO2S/c1-2-12-8-5-3-4-7(6-8)9(10)11/h3-6,10-11H,2H2,1H3
InChI key:InChIKey=CZODYJDCHKOBID-UHFFFAOYSA-N
SMILES:S(CC)C1=CC(B(O)O)=CC=C1
Synonyms:
  • 3-(Ethylthio)Phenylboronic Acid
  • 3-Ethylsulfanylphenylboronic acid
  • B-[3-(Ethylthio)phenyl]boronic acid
  • Boronic acid, B-[3-(ethylthio)phenyl]-
  • Boronic acid, [3-(ethylthio)phenyl]-
  • [3-(Ethylthio)phenyl]boronic acid
  • [3-(Ethylsulfanyl)phenyl]boronic acid
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