(1-(tert-Butoxycarbonyl)-1H-pyrrolo[3,2-c]pyridin-2-yl)boronic acid

• CAT Number: L021865
• CAS Number: 1373273-47-2
• Molecular Formula: C12H15BN2O4
• Molecular Weight: 262.07
• Purity: ≥95%
• IUPAC Name: [1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolo[3,2-c]pyridin-2-yl]boronic acid
• InChI: InChI=1S/C12H15BN2O4/c1-12(2,3)19-11(16)15-9-4-5-14-7-8(9)6-10(15)13(17)18/h4-7,17-18H,1-3H3
• InChIKey: KRXKAIXWQKYUFQ-UHFFFAOYSA-N

(1-(tert-Butoxycarbonyl)-1H-pyrrolo[3,2-c]pyridin-2-yl)boronic acid(CAT: L021865) is a boronic acid derivative featuring a pyrrolo[3,2-c]pyridine ring system with a tert-butoxycarbonyl (Boc) protecting group attached to the nitrogen atom and a boronic acid group at the 2-position. This compound is particularly useful in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions, where the boronic acid functionality allows for the formation of carbon-carbon bonds. The Boc group serves as a protective group for the nitrogen during chemical reactions, providing stability while allowing for selective deprotection when needed. This compound is often employed in medicinal chemistry for the synthesis of bioactive molecules, such as kinase inhibitors or small-molecule modulators. Its structure makes it a versatile building block in the development of complex pharmaceutical agents.