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CAS 874289-49-3

:

B-[2-Fluoro-5-[[(1-methylethyl)amino]carbonyl]phenyl]boronic acid

Description:
B-[2-Fluoro-5-[[(1-methylethyl)amino]carbonyl]phenyl]boronic acid, with the CAS number 874289-49-3, is a boronic acid derivative characterized by its unique functional groups that include a fluorine atom and an isopropylamino carbonyl moiety. 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 medicinal chemistry and organic synthesis. The presence of the fluorine atom can enhance the compound's lipophilicity and influence its biological activity. Additionally, the boronic acid group is known for its role in the development of inhibitors for certain enzymes, particularly in the context of cancer research. The compound's structure suggests potential interactions with biological targets, which may be explored for therapeutic purposes. Overall, B-[2-Fluoro-5-[[(1-methylethyl)amino]carbonyl]phenyl]boronic acid represents a valuable chemical entity in the field of drug discovery and development.
Formula:C10H13BFNO3
InChI:InChI=1S/C10H13BFNO3/c1-6(2)13-10(14)7-3-4-9(12)8(5-7)11(15)16/h3-6,15-16H,1-2H3,(H,13,14)
InChI key:InChIKey=NCRUGKRIPMSQHI-UHFFFAOYSA-N
SMILES:C(NC(C)C)(=O)C1=CC(B(O)O)=C(F)C=C1
Synonyms:
  • [2-Fluoro-5-(isopropylcarbamoyl)phenyl]boronic acid
  • [2-Fluoro-5-[(propan-2-yl)carbamoyl]phenyl]boronic acid
  • B-[2-Fluoro-5-[[(1-methylethyl)amino]carbonyl]phenyl]boronic acid
  • Boronic acid, B-[2-fluoro-5-[[(1-methylethyl)amino]carbonyl]phenyl]-
  • Boronic acid, [2-fluoro-5-[[(1-methylethyl)amino]carbonyl]phenyl]-
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