(2-Methyl-1,3-benzoxazol-6-yl)boronic acid

• CAT Number: L038982
• CAS Number: 866332-15-2
• Molecular Formula: C8H8BNO3
• Molecular Weight: 176.97
• Purity: ≥95%
• IUPAC Name: (2-methyl-1,3-benzoxazol-6-yl)boronic acid
• InChI: InChI=1S/C8H8BNO3/c1-5-10-7-3-2-6(9(11)12)4-8(7)13-5/h2-4,11-12H,1H3
• InChIKey: MFPJERIVTFQLEG-UHFFFAOYSA-N
• SMILES: B(C1=CC2=C(C=C1)N=C(O2)C)(O)O

(2-Methyl-1,3-benzoxazol-6-yl)boronic acid(CAT: L038982) is a high-purity boronic acid derivative featuring a benzoxazole core with a methyl group at the 2-position and a boronic acid functionality at the 6-position. This versatile compound is widely employed as a key intermediate in pharmaceutical research and organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions for the construction of complex bioactive molecules, heterocyclic frameworks, and functional materials. The boronic acid group enables precise chemical modifications, while the benzoxazole core imparts stability and biological relevance. (2-Methyl-1,3-benzoxazol-6-yl)boronic acid is an essential building block for advanced medicinal chemistry, agrochemicals, and material science applications.