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CAS 850568-10-4

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B-[3-(Aminothioxomethyl)phenyl]boronic acid

Description:
B-[3-(Aminothioxomethyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that features an aminothioxomethyl substituent. 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 aminothioxomethyl group introduces additional reactivity and potential for biological activity, which may enhance its utility in drug development or as a biochemical probe. The compound is likely to be soluble in polar solvents, and its reactivity can be influenced by pH and the presence of other functional groups. As with many boronic acids, it may also participate in Suzuki coupling reactions, facilitating the formation of carbon-carbon bonds in organic synthesis. Safety and handling precautions should be observed, as with all chemical substances, particularly those with reactive functional groups.
Formula:C7H8BNO2S
InChI:InChI=1S/C7H8BNO2S/c9-7(12)5-2-1-3-6(4-5)8(10)11/h1-4,10-11H,(H2,9,12)
InChI key:InChIKey=ZPKLUYJBCAHWIW-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(C(N)=S)=CC=C1
Synonyms:
  • B-[3-(Aminothioxomethyl)phenyl]boronic acid
  • 3-(Aminothiocarbonyl)phenylboronic acid
  • Boronic acid, B-[3-(aminothioxomethyl)phenyl]-
  • Boronic acid, [3-(aminothioxomethyl)phenyl]-
  • (3-Carbamothioylphenyl)boronic acid
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