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CAS 871333-02-7

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B-[3-Methoxy-5-(4-morpholinylsulfonyl)phenyl]boronic acid

Description:
B-[3-Methoxy-5-(4-morpholinylsulfonyl)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. This compound features a phenyl ring substituted with a methoxy group and a morpholinylsulfonyl group, contributing to its unique chemical properties and potential biological activity. The morpholine moiety may enhance solubility and bioavailability, while the sulfonyl group can influence the compound's reactivity and interaction with biological targets. Typically, boronic acids are utilized in medicinal chemistry for drug development and as intermediates in organic synthesis. The compound's specific characteristics, such as solubility, stability, and reactivity, can vary based on environmental conditions and the presence of other functional groups. Overall, B-[3-Methoxy-5-(4-morpholinylsulfonyl)phenyl]boronic acid represents a versatile structure with potential applications in pharmaceuticals and materials science.
Formula:C11H16BNO6S
InChI:InChI=1S/C11H16BNO6S/c1-18-10-6-9(12(14)15)7-11(8-10)20(16,17)13-2-4-19-5-3-13/h6-8,14-15H,2-5H2,1H3
InChI key:InChIKey=SSOACLYCMHIOGQ-UHFFFAOYSA-N
SMILES:S(=O)(=O)(C1=CC(B(O)O)=CC(OC)=C1)N2CCOCC2
Synonyms:
  • B-[3-Methoxy-5-(4-morpholinylsulfonyl)phenyl]boronic acid
  • Boronic acid, [3-methoxy-5-(4-morpholinylsulfonyl)phenyl]-
  • Boronic acid, B-[3-methoxy-5-(4-morpholinylsulfonyl)phenyl]-
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