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CAS 2121515-18-0

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B-[3-Bromo-5-[(methylamino)carbonyl]phenyl]boronic acid

Description:
B-[3-Bromo-5-[(methylamino)carbonyl]phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols and is widely used in organic synthesis and medicinal chemistry. The compound features a bromine atom and a methylamino carbonyl group attached to a phenyl ring, contributing to its reactivity and potential applications in drug development and materials science. The boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the presence of the bromine substituent can enhance the electrophilicity of the aromatic system, facilitating further chemical transformations. This compound may also exhibit interesting biological properties, although specific biological activity would need to be evaluated through experimental studies. Overall, B-[3-Bromo-5-[(methylamino)carbonyl]phenyl]boronic acid represents a versatile building block in synthetic organic chemistry.
Formula:C8H9BBrNO3
InChI:InChI=1S/C8H9BBrNO3/c1-11-8(12)5-2-6(9(13)14)4-7(10)3-5/h2-4,13-14H,1H3,(H,11,12)
InChI key:InChIKey=OHDDEMWGXPFMHZ-UHFFFAOYSA-N
SMILES:C(NC)(=O)C1=CC(B(O)O)=CC(Br)=C1
Synonyms:
  • Boronic acid, B-[3-bromo-5-[(methylamino)carbonyl]phenyl]-
  • B-[3-Bromo-5-[(methylamino)carbonyl]phenyl]boronic acid
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