3-(N-BOC-N-Butylamino)phenylboronic acid

• CAT Number: R039308
• CAS Number: 925932-71-4
• Molecular Formula: C15H24BNO4
• Molecular Weight: 293.17
• Purity: ≥95%
• Storage: -20°C
• IUPAC Name: [3-[butyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]phenyl]boronic acid
• InChI: InChI=1S/C15H24BNO4/c1-5-6-10-17(14(18)21-15(2,3)4)13-9-7-8-12(11-13)16(19)20/h7-9,11,19-20H,5-6,10H2,1-4H3
• InChIKey: PWGLYYWIKQFCSS-UHFFFAOYSA-N
• SMILES: B(C1=CC(=CC=C1)N(CCCC)C(=O)OC(C)(C)C)(O)O

3-(N-BOC-N-Butylamino)phenylboronic acid is an organic compound featuring a boronic acid group attached to a phenyl ring, with a butylamino group protected by a BOC (tert-butoxycarbonyl) group. This compound is valuable in organic synthesis, particularly in the formation of C-C bonds through Suzuki-Miyaura coupling reactions. Its boronic acid moiety enables its use in cross-coupling reactions, while the BOC-protected butylamino group allows selective functionalization in peptide synthesis and medicinal chemistry. Researchers employ 3-(N-BOC-N-Butylamino)phenylboronic acid in drug development and the design of bioactive molecules for therapeutic and diagnostic applications.