CAS 948593-64-4

B-(3-Amino-5-chloro-2-pyridinyl)boronic acid

Description:

B-(3-Amino-5-chloro-2-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that contains an amino and a chloro substituent. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar solvents like water and methanol, and may have moderate stability under standard conditions. The boronic acid moiety allows for participation in various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis and medicinal chemistry. The amino group can engage in hydrogen bonding and may influence the compound's reactivity and interaction with biological targets. Additionally, the presence of the chlorine atom can affect the electronic properties of the molecule, potentially enhancing its biological activity or selectivity. Overall, B-(3-Amino-5-chloro-2-pyridinyl)boronic acid is a versatile compound with applications in drug development and material science.

Formula: C₅H₆BClN₂O₂

InChI: InChI=1S/C5H6BClN2O2/c7-3-1-4(8)5(6(10)11)9-2-3/h1-2,10-11H,8H2

InChI key: InChIKey=QMQBKEZDGSJLIR-UHFFFAOYSA-N

SMILES: B(O)(O)C1=C(N)C=C(Cl)C=N1

Synonyms:

• Boronic acid, B-(3-amino-5-chloro-2-pyridinyl)-
• 3-Amino-5-chloropyridin-2-ylboronic acid
• B-(3-Amino-5-chloro-2-pyridinyl)boronic acid
• (3-Amino-5-chloropyridin-2-yl)boronic acid