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CAS 1217501-06-8

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B-[4-(Cyclopropylsulfinyl)phenyl]boronic acid

Description:
B-[4-(Cyclopropylsulfinyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a cyclopropylsulfinyl group. This compound typically exhibits properties such as being a white to off-white solid, with solubility in polar solvents like water and alcohols, which is common for boronic acids due to their ability to form hydrogen bonds. The presence of the sulfinyl group enhances its reactivity and may influence its biological activity, making it of interest in medicinal chemistry. Boronic acids are known for their ability to form reversible covalent bonds with diols, which is a key feature in applications such as drug development and organic synthesis. Additionally, this compound may participate in Suzuki coupling reactions, a widely used method for forming carbon-carbon bonds in organic synthesis. Its specific applications and reactivity can vary based on the substituents and the overall molecular structure.
Formula:C9H11BO3S
InChI:InChI=1S/C9H11BO3S/c11-10(12)7-1-3-8(4-2-7)14(13)9-5-6-9/h1-4,9,11-12H,5-6H2
InChI key:InChIKey=UVAFNQYMJVLTNA-UHFFFAOYSA-N
SMILES:S(=O)(C1CC1)C2=CC=C(B(O)O)C=C2
Synonyms:
  • [4-(Cyclopropylsulfinyl)phenyl]boronic acid
  • B-[4-(Cyclopropylsulfinyl)phenyl]boronic acid
  • Boronic acid, B-[4-(cyclopropylsulfinyl)phenyl]-
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