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CAS 1137339-95-7

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B-[2-Methoxy-5-[(methylamino)carbonyl]phenyl]boronic acid

Description:
B-[2-Methoxy-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, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a methoxy group and a methylamino carbonyl substituent on a phenyl ring, contributing to its solubility and reactivity. The boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. Additionally, the presence of the methylamino group may enhance its biological activity, potentially making it relevant in drug development. The compound is typically a white to off-white solid and is soluble in polar organic solvents. Its stability and reactivity can be influenced by pH and the presence of other functional groups, making it a versatile building block in synthetic chemistry. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C9H12BNO4
InChI:InChI=1S/C9H12BNO4/c1-11-9(12)6-3-4-8(15-2)7(5-6)10(13)14/h3-5,13-14H,1-2H3,(H,11,12)
InChI key:InChIKey=KCLKEUZCMVHJLZ-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(OC)C=CC(C(NC)=O)=C1
Synonyms:
  • B-[2-Methoxy-5-[(methylamino)carbonyl]phenyl]boronic acid
  • [2-Methoxy-5-(methylcarbamoyl)phenyl]boronic acid
  • 2-Methoxy-5-(methylaminocarbonyl)phenylboronic acid
  • Boronic acid, B-[2-methoxy-5-[(methylamino)carbonyl]phenyl]-
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