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CAS 480438-52-6

:

B-[1-(Phenylsulfonyl)-1H-indol-6-yl]boronic acid

Description:
B-[1-(Phenylsulfonyl)-1H-indol-6-yl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features an indole ring, which is a bicyclic structure consisting of a benzene fused to a pyrrole, contributing to its aromatic properties and potential biological activity. The phenylsulfonyl group enhances its solubility and reactivity, making it useful in various chemical reactions, including Suzuki coupling reactions, which are pivotal in the synthesis of complex organic molecules. The boronic acid moiety also plays a significant role in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific biological pathways. Additionally, this compound may exhibit unique physical properties such as melting point, solubility, and stability, which are essential for its application in research and industry. Overall, B-[1-(Phenylsulfonyl)-1H-indol-6-yl]boronic acid is a versatile compound with significant implications in organic synthesis and drug development.
Formula:C14H12BNO4S
InChI:InChI=1S/C14H12BNO4S/c17-15(18)12-7-6-11-8-9-16(14(11)10-12)21(19,20)13-4-2-1-3-5-13/h1-10,17-18H
InChI key:InChIKey=RVWRLLZYYUIBOX-UHFFFAOYSA-N
SMILES:S(=O)(=O)(N1C=2C(C=C1)=CC=C(B(O)O)C2)C3=CC=CC=C3
Synonyms:
  • 1-Phenylsulfonylindol-6-ylboronic acid
  • Boronic acid, [1-(phenylsulfonyl)-1H-indol-6-yl]-
  • Boronic acid, B-[1-(phenylsulfonyl)-1H-indol-6-yl]-
  • (1-(Phenylsulfonyl)-1H-indol-6-yl)boronic acid
  • B-[1-(Phenylsulfonyl)-1H-indol-6-yl]boronic acid
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