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CAS 480438-51-5

:

B-[1-(Phenylsulfonyl)-1H-indol-5-yl]boronic acid

Description:
B-[1-(Phenylsulfonyl)-1H-indol-5-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 structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring, contributing to its aromatic properties. The phenylsulfonyl group enhances its reactivity and solubility in organic solvents, making it useful in various chemical reactions, including Suzuki coupling reactions, which are pivotal in the synthesis of biaryl compounds. The boronic acid moiety also plays a significant role in medicinal chemistry, particularly in the development of pharmaceuticals, due to its ability to interact with biological targets. Additionally, this compound may exhibit specific biological activities, although detailed studies would be necessary to elucidate its pharmacological profile. Overall, B-[1-(Phenylsulfonyl)-1H-indol-5-yl]boronic acid is a versatile compound with applications in organic synthesis and potential therapeutic uses.
Formula:C14H12BNO4S
InChI:InChI=1S/C14H12BNO4S/c17-15(18)12-6-7-14-11(10-12)8-9-16(14)21(19,20)13-4-2-1-3-5-13/h1-10,17-18H
InChI key:InChIKey=QBWYPMYEBNWOFW-UHFFFAOYSA-N
SMILES:S(=O)(=O)(N1C=2C(C=C1)=CC(B(O)O)=CC2)C3=CC=CC=C3
Synonyms:
  • Boronic acid, [1-(phenylsulfonyl)-1H-indol-5-yl]-
  • B-[1-(Phenylsulfonyl)-1H-indol-5-yl]boronic acid
  • Boronic acid, B-[1-(phenylsulfonyl)-1H-indol-5-yl]-
  • 1-(Phenylsulphonyl)-1H-indole-5-boronic acid
  • 1-Phenylsulfonylindole-5-boronic acid
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