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CAS 690957-44-9

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B-[4-[(Phenylamino)methyl]phenyl]boronic acid

Description:
B-[4-[(Phenylamino)methyl]phenyl]boronic acid, identified by its CAS number 690957-44-9, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a phenylamino group. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar organic solvents, and possessing moderate stability under standard laboratory conditions. The boronic acid moiety allows for reversible interactions with diols, making it useful in various applications, including medicinal chemistry and materials science. It may also play a role in Suzuki coupling reactions, which are essential for forming carbon-carbon bonds in organic synthesis. Additionally, the presence of the phenylamino group can influence the compound's electronic properties and reactivity, potentially enhancing its biological activity or selectivity in targeted applications. Overall, B-[4-[(Phenylamino)methyl]phenyl]boronic acid is a versatile compound with significant implications in both research and industrial contexts.
Formula:C13H14BNO2
InChI:InChI=1S/C13H14BNO2/c16-14(17)12-8-6-11(7-9-12)10-15-13-4-2-1-3-5-13/h1-9,15-17H,10H2
InChI key:InChIKey=FHQIDGWZDOKKDI-UHFFFAOYSA-N
SMILES:C(NC1=CC=CC=C1)C2=CC=C(B(O)O)C=C2
Synonyms:
  • Boronic acid, [4-[(phenylamino)methyl]phenyl]-
  • (4-((Phenylamino)methyl)phenyl)boronicacid
  • B-[4-[(Phenylamino)methyl]phenyl]boronic acid
  • Boronic acid, B-[4-[(phenylamino)methyl]phenyl]-
  • [4-[(Phenylamino)methyl]phenyl]boronic acid
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