N-Boc-pyrryl-boronic Acid

• CAT Number: R002425
• CAS Number: 135884-31-0
• Molecular Formula: C9H14BNO4
• Molecular Weight: 211.024
• Purity: ≥95%
• Synonyms: N-Boc-2-pyrroleboronic Acid; 2-Borono-1H-pyrrole-1-carboxylic Acid 1-(1,1-Dimethylethyl) Ester; (1-(tert-Butoxycarbonyl)pyrrole-2-yl)boronic Acid; [1-[[(1,1-Dimethylethyl)oxy]carbonyl]-1H-pyrrol-2-yl]boronic Acid
• Storage: -20°C
• IUPAC Name: [1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrol-2-yl]boronic acid
• InChI: InChI=1S/C9H14BNO4/c1-9(2,3)15-8(12)11-6-4-5-7(11)10(13)14/h4-6,13-14H,1-3H3
• InChIKey: ZWGMJLNXIVRFRJ-UHFFFAOYSA-N
• SMILES: B(C1=CC=CN1C(=O)OC(C)(C)C)(O)O

N-Boc-pyrryl-boronic Acid(CAT: R002425) is a significant compound in organic chemistry. It belongs to the class of boronic acids, renowned for their utility in Suzuki-Miyaura cross-coupling reactions. This compound features a Boc (tert-butoxycarbonyl) protecting group, which enhances its stability during synthesis. In organic chemistry, it serves as a crucial reagent for building complex organic molecules, especially in the synthesis of pharmaceuticals and agrochemicals. Its boronic acid functionality enables it to form bonds with aryl or vinyl halides, making it indispensable in various carbon-carbon bond-forming reactions.