(3-(Di-p-tolylamino)phenyl)boronic acid

• CAT Number: L007859
• CAS Number: 1162753-18-5
• Molecular Formula: C20H20BNO2
• Molecular Weight: 317.2
• Purity: ≥95%
• Storage: 2-8°C
• IUPAC Name: [3-(4-methyl-N-(4-methylphenyl)anilino)phenyl]boronic acid
• InChI: InChI=1S/C20H20BNO2/c1-15-6-10-18(11-7-15)22(19-12-8-16(2)9-13-19)20-5-3-4-17(14-20)21(23)24/h3-14,23-24H,1-2H3
• InChIKey: CISBNIQSSKGQSN-UHFFFAOYSA-N
• SMILES: B(C1=CC(=CC=C1)N(C2=CC=C(C=C2)C)C3=CC=C(C=C3)C)(O)O

(3-(Di-p-alkylamino)phenyl)boronic acid（Cat No.:L007859）. It is a boronic acid derivative featuring a boron atom attached to a phenyl ring, which is further substituted with a di-p-alkylamino group at the 3-position. Boronic acids like this one are important in organic synthesis, particularly in Suzuki-Miyaura coupling reactions, enabling the formation of carbon-carbon bonds. Compounds with similar structures are vital in medicinal chemistry, serving as key intermediates for drug discovery and development. This specific compound’s unique arrangement of atoms makes it valuable for the synthesis of diverse organic molecules with potential applications in pharmaceuticals and materials science.