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CAS 871332-99-9

:

B-[5-[(Dimethylamino)sulfonyl]-2-methylphenyl]boronic acid

Description:
B-[5-[(Dimethylamino)sulfonyl]-2-methylphenyl]boronic acid, with the CAS number 871332-99-9, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group that is further substituted with a dimethylaminosulfonyl group and a methyl group. 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 organic synthesis and medicinal chemistry. The dimethylamino group enhances its solubility in organic solvents and may influence its biological activity. Additionally, the sulfonyl group can impart unique reactivity and stability characteristics. The compound's structure suggests potential applications in drug development, particularly in the design of inhibitors for certain enzymes or in the development of targeted therapies. Overall, its unique functional groups contribute to its chemical reactivity and potential utility in various fields of research.
Formula:C9H14BNO4S
InChI:InChI=1/C9H14BNO4S/c1-7-4-5-8(6-9(7)10(12)13)16(14,15)11(2)3/h4-6,12-13H,1-3H3
InChI key:InChIKey=ISKRAODOAGHCKV-UHFFFAOYSA-N
SMILES:S(N(C)C)(=O)(=O)C1=CC(B(O)O)=C(C)C=C1
Synonyms:
  • (5-(N,N-Dimethylsulfamoyl)-2-methylphenyl)boronicacid
  • B-[5-[(Dimethylamino)sulfonyl]-2-methylphenyl]boronic acid
  • Boronic acid, B-[5-[(dimethylamino)sulfonyl]-2-methylphenyl]-
  • Boronic acid, [5-[(dimethylamino)sulfonyl]-2-methylphenyl]-
  • [5-(Dimethylsulfamoyl)-2-methylphenyl]boronic acid
  • [5-(N,N-Dimethylsulfamoyl)-2-methylphenyl]boronic acid
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