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CAS 913835-61-7

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B-[4-[(Hydroxyamino)iminomethyl]phenyl]boronic acid

Description:
B-[4-[(Hydroxyamino)iminomethyl]phenyl]boronic acid, with the CAS number 913835-61-7, is a boronic acid derivative characterized by its unique functional groups that include a boron atom bonded to a phenyl ring and an amino group. 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 organic synthesis and medicinal chemistry. The presence of the hydroxyamino group enhances its reactivity and potential for forming complexes with biomolecules. Additionally, boronic acids are known for their role in the Suzuki coupling reaction, a key method in the formation of carbon-carbon bonds. The compound's solubility and stability can vary depending on the pH and the presence of other functional groups. Overall, B-[4-[(Hydroxyamino)iminomethyl]phenyl]boronic acid is a versatile compound with potential applications in drug development and materials science due to its unique chemical properties.
Formula:C7H9BN2O3
InChI:InChI=1S/C7H9BN2O3/c9-7(10-13)5-1-3-6(4-2-5)8(11)12/h1-4,11-13H,(H2,9,10)
InChI key:InChIKey=LTKQMNXFUOIBQG-UHFFFAOYSA-N
SMILES:C(NO)(=N)C1=CC=C(B(O)O)C=C1
Synonyms:
  • Boronic acid, B-[4-[(hydroxyamino)iminomethyl]phenyl]-
  • B-[4-[(Hydroxyamino)iminomethyl]phenyl]boronic acid
  • Boronic acid, [4-[(hydroxyamino)iminomethyl]phenyl]-
  • (4-(N′-Hydroxycarbamimidoyl)phenyl)boronic acid
  • [4-(N-Hydroxycarbamimidoyl)phenyl]boronic acid
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