(2-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol

• CAT Number: L027576
• CAS Number: 1051316-34-7
• Molecular Formula: C13H18BClO3
• Molecular Weight: 268.54
• Purity: ≥95%
• IUPAC Name: [2-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanol
• InChI: InChI=1S/C13H18BClO3/c1-12(2)13(3,4)18-14(17-12)10-6-5-9(8-16)11(15)7-10/h5-7,16H,8H2,1-4H3
• InChIKey: BLQXWYINFTVLEL-UHFFFAOYSA-N
• SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CC(=C(C=C2)CO)Cl

(2-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol(CAT: L027576) is a high-purity compound widely utilized in pharmaceutical and chemical research. Featuring a boronic ester group, a chlorinated aromatic ring, and a hydroxymethyl functionality, this compound serves as a versatile intermediate in organic synthesis. It is particularly valuable for Suzuki-Miyaura cross-coupling reactions, enabling the development of complex bioactive molecules and advanced materials. Its unique structure allows for precise modifications in drug discovery and material science applications. With consistent quality and reactivity, (2-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)methanol is a reliable tool for advancing innovative research in various scientific fields.