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CAS 871329-69-0

:

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

Description:
B-[4-(4-Thiomorpholinylsulfonyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. The compound features a phenyl ring substituted with a thiomorpholine sulfonyl group, which enhances its solubility and reactivity. This structure contributes to its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. The thiomorpholine moiety may also impart unique properties, such as increased lipophilicity or specific interactions with biological targets. Additionally, boronic acids are often utilized in the synthesis of complex organic molecules and as intermediates in the production of agrochemicals. Overall, B-[4-(4-Thiomorpholinylsulfonyl)phenyl]boronic acid is a versatile compound with significant implications in synthetic organic chemistry and drug development.
Formula:C10H14BNO4S2
InChI:InChI=1S/C10H14BNO4S2/c13-11(14)9-1-3-10(4-2-9)18(15,16)12-5-7-17-8-6-12/h1-4,13-14H,5-8H2
InChI key:InChIKey=ROGGFXZKSGGVQE-UHFFFAOYSA-N
SMILES:S(=O)(=O)(C1=CC=C(B(O)O)C=C1)N2CCSCC2
Synonyms:
  • (4-(Thiomorpholinosulfonyl)phenyl)boronic acid
  • (4-(Thiomorpholinosulfonyl)phenyl)boronicacid
  • B-[4-(4-Thiomorpholinylsulfonyl)phenyl]boronic acid
  • Boronic acid, B-[4-(4-thiomorpholinylsulfonyl)phenyl]-
  • Boronic acid, [4-(4-thiomorpholinylsulfonyl)phenyl]-
  • [4-(Thiomorpholin-4-ylsulphonyl)phenyl]boronic acid
  • [4-(Thiomorpholine-4-sulfonyl)phenyl]boronic acid
  • [4-[(4-Thiomorpholinyl)sulfonyl]phenyl]boronic acid
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