2-(4-(2-(2-Methoxyethoxy)ethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

• CAT Number: L023513
• CAS Number: 1366602-62-1
• Molecular Formula: C17H27BO5
• Molecular Weight: 322.20
• Purity: ≥95%
• IUPAC Name: 2-[4-[2-(2-methoxyethoxy)ethoxy]phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• InChI: InChI=1S/C17H27BO5/c1-16(2)17(3,4)23-18(22-16)14-6-8-15(9-7-14)21-13-12-20-11-10-19-5/h6-9H,10-13H2,1-5H3
• InChIKey: VAIZYGOXWWZRDO-UHFFFAOYSA-N
• SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC=C(C=C2)OCCOCCOC

2-(4-(2-(2-Methoxyethoxy)ethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane（Cat No.:L023513）is a boronic ester widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. The compound features a dioxaborolane ring with a phenyl group substituted by a triethylene glycol chain, enhancing its solubility and reactivity. It is a crucial intermediate in the development of pharmaceuticals, polymers, and advanced materials. With high stability and precise functionality, 2-(4-(2-(2-Methoxyethoxy)ethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is essential for efficient chemical transformations and innovative research applications in various fields.