Methyl 2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

• CAT Number: L040349
• CAS Number: 478375-39-2
• Molecular Formula: C15H21BO4
• Molecular Weight: 276.14
• Purity: ≥95%
• IUPAC Name: methyl 2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate
• InChI: InChI=1S/C15H21BO4/c1-10-7-8-11(9-12(10)13(17)18-6)16-19-14(2,3)15(4,5)20-16/h7-9H,1-6H3
• InChIKey: WBHBKJFHYGIUQU-UHFFFAOYSA-N
• SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC(=C(C=C2)C)C(=O)O

Methyl 2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate(CAT: L040349) is a high-purity boronic ester derivative featuring a methylbenzoate core functionalized with a boronate group at the 5-position and a methyl substituent at the 2-position. This compound serves as a critical intermediate in pharmaceutical research and organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions for constructing complex molecules, including bioactive compounds and functional materials. Its boronic ester functionality ensures excellent stability and reactivity, enabling precise transformations for medicinal chemistry, agrochemicals, and material science applications. Methyl 2-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate is ideal for precision-driven synthetic strategies.