2-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetic acid

• CAT Number: L036300
• CAS Number: 1072945-02-8
• Molecular Formula: C14H19BO4
• Molecular Weight: 262.11
• Purity: ≥95%
• IUPAC Name: 2-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetic acid
• InChI: InChI=1S/C14H19BO4/c1-13(2)14(3,4)19-15(18-13)11-8-6-5-7-10(11)9-12(16)17/h5-8H,9H2,1-4H3,(H,16,17)
• InChIKey: XQNYGTSLIDQFRG-UHFFFAOYSA-N

2-(2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetic acid(CAT: L036300) is an organoboron compound widely used in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions. This molecule features a boronic ester (dioxaborolane) group attached to a phenyl ring, which, in turn, is linked to an acetic acid group. The boronic ester provides stability and reactivity for palladium-catalyzed coupling, making it a valuable building block for creating biaryl compounds, which are common in pharmaceutical and materials chemistry. Additionally, the acetic acid group enhances solubility and reactivity in aqueous media, allowing for further derivatization. This compound is instrumental in synthesizing complex molecules, such as bioactive compounds and advanced materials, due to its versatility and compatibility with various reaction conditions.