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CAS 1451391-89-1

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B-[2-Chloro-4-[(methylamino)carbonyl]phenyl]boronic acid

Description:
B-[2-Chloro-4-[(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 chlorinated phenyl ring, which enhances its reactivity and potential for biological activity. The methylamino group contributes to its solubility and may influence its interaction with biological targets. This compound is typically utilized in the development of pharmaceuticals, particularly in the synthesis of compounds that inhibit specific enzymes or receptors. Its boronic acid moiety is particularly valuable in the context of drug design, as it can participate in various chemical reactions, including Suzuki coupling, which is essential for constructing complex organic molecules. Overall, B-[2-Chloro-4-[(methylamino)carbonyl]phenyl]boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C8H9BClNO3
InChI:InChI=1S/C8H9BClNO3/c1-11-8(12)5-2-3-6(9(13)14)7(10)4-5/h2-4,13-14H,1H3,(H,11,12)
InChI key:InChIKey=LSMHGCJWZPHACP-UHFFFAOYSA-N
SMILES:C(NC)(=O)C1=CC(Cl)=C(B(O)O)C=C1
Synonyms:
  • B-[2-Chloro-4-[(methylamino)carbonyl]phenyl]boronic acid
  • Boronic acid, B-[2-chloro-4-[(methylamino)carbonyl]phenyl]-
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