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CAS 1072945-62-0

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B-[4-[(Ethylsulfonyl)amino]phenyl]boronic acid

Description:
B-[4-[(Ethylsulfonyl)amino]phenyl]boronic acid, with the CAS number 1072945-62-0, is a boronic acid derivative characterized by its boron atom bonded to a phenyl group and an ethylsulfonylamino substituent. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including drug development and materials science. The presence of the ethylsulfonyl group enhances its solubility and reactivity, contributing to its potential as a pharmacophore in medicinal chemistry. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in organic synthesis for forming carbon-carbon bonds. The compound's structure suggests it may also exhibit biological activity, particularly in targeting specific enzymes or receptors. Overall, B-[4-[(Ethylsulfonyl)amino]phenyl]boronic acid represents a versatile chemical entity with significant implications in both synthetic and medicinal chemistry.
Formula:C8H12BNO4S
InChI:InChI=1S/C8H12BNO4S/c1-2-15(13,14)10-8-5-3-7(4-6-8)9(11)12/h3-6,10-12H,2H2,1H3
InChI key:InChIKey=DFGZKFSYJUXPOK-UHFFFAOYSA-N
SMILES:N(S(CC)(=O)=O)C1=CC=C(B(O)O)C=C1
Synonyms:
  • (4-(Ethylsulfonamido)phenyl)boronicacid
  • B-[4-[(Ethylsulfonyl)amino]phenyl]boronic acid
  • Boronic acid, B-[4-[(ethylsulfonyl)amino]phenyl]-
  • (4-Ethanesulfonamidophenyl)boronic acid
  • 4-(Ethylsulfonylamino)phenylboronic acid
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