3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-YL)-1-[tris(1-methylethyl)silyl]-1H-pyrrole

• CAT Number: L035728
• CAS Number: 365564-11-0
• Molecular Formula: C19H36BNO2Si
• Molecular Weight: 349.41
• Purity: ≥95%
• IUPAC Name: tri(propan-2-yl)-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrrol-1-yl]silane
• InChI: InChI=1S/C19H36BNO2Si/c1-14(2)24(15(3)4,16(5)6)21-12-11-17(13-21)20-22-18(7,8)19(9,10)23-20/h11-16H,1-10H3
• InChIKey: GWFIZBYDIHGZRJ-UHFFFAOYSA-N
• SMILES: B1(OC(C(O1)(C)C)(C)C)C2=CN(C=C2)[Si](C(C)C)(C(C)C)C(C)C

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1-[tris(1-methylethyl)silyl]-1H-pyrrole(CAT: L035728) is a high-purity compound widely utilized in pharmaceutical and synthetic chemistry research. This boron-containing pyrrole derivative, featuring a triisopropylsilyl (TIPS) protective group, is a versatile intermediate for the synthesis of complex organic molecules. Its unique structure supports applications in cross-coupling reactions, medicinal chemistry, and material science. The boronic ester functionality allows for efficient incorporation into Suzuki-Miyaura coupling reactions, enabling the construction of diverse molecular frameworks. With excellent stability and reactivity, this compound is a valuable tool for researchers advancing drug discovery, innovative material design, and synthetic methodologies.