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CAS 850568-39-7

:

B-[3-[[(Methylsulfonyl)amino]methyl]phenyl]boronic acid

Description:
B-[3-[[(Methylsulfonyl)amino]methyl]phenyl]boronic acid, with the CAS number 850568-39-7, is a boronic acid derivative characterized by its unique functional groups, which include a boron atom bonded to a phenyl ring and a methylsulfonylamino group. This compound typically exhibits properties such as moderate solubility in polar solvents, making it useful in various chemical reactions, particularly in organic synthesis and medicinal chemistry. The presence of the boronic acid moiety allows for participation in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds. Additionally, the methylsulfonyl group can enhance the compound's biological activity and solubility profile. This compound may also exhibit potential as a pharmaceutical intermediate or in the development of targeted therapies due to its ability to interact with biological molecules. Overall, its structural features contribute to its reactivity and applicability in diverse chemical contexts.
Formula:C8H12BNO4S
InChI:InChI=1S/C8H12BNO4S/c1-15(13,14)10-6-7-3-2-4-8(5-7)9(11)12/h2-5,10-12H,6H2,1H3
InChI key:InChIKey=FJSWJJOLFPIDER-UHFFFAOYSA-N
SMILES:C(NS(C)(=O)=O)C1=CC(B(O)O)=CC=C1
Synonyms:
  • (3-(Methylsulfonamidomethyl)phenyl)boronic acid
  • (3-(Methylsulfonamidomethyl)phenyl)boronicacid
  • B-[3-[[(Methylsulfonyl)amino]methyl]phenyl]boronic acid
  • Boronic acid, B-[3-[[(methylsulfonyl)amino]methyl]phenyl]-
  • Boronic acid, [3-[[(methylsulfonyl)amino]methyl]phenyl]-
  • [3-(Methanesulfonamidomethyl)phenyl]boronic acid
  • [3-(Methanesulfonylaminomethyl)phenyl]boronic acid
  • [3-[[(Methylsulfonyl)amino]methyl]phenyl]boronic acid
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