900989

1,3,5-Phenyltriboronic acid, tris(pinacol) ester

≥97%

• Sinónimos: 1,3,5-Tris(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene
• Fórmula empírica (notación de Hill): C₂₄H₃₉B₃O₆
• Número de CAS: 365564-05-2
• Peso molecular: 456.00
• Número MDL: MFCD17167305
• Código UNSPSC: 12352106
• NACRES: NA.06

Propiedades

• Nivel de calidad: 100
• Ensayo: ≥97%
• Formulario: powder or crystals
• mp: 286-287 °C
• cadena SMILES: CC1(C)OB(OC1(C)C)C2=CC(B3OC(C)(C)C(C)(C)O3)=CC(B4OC(C)(C)C(C)(C)O4)=C2
• InChI: 1S/C24H39B3O6/c1-19(2)20(3,4)29-25(28-19)16-13-17(26-30-21(5,6)22(7,8)31-26)15-18(14-16)27-32-23(9,10)24(11,12)33-27/h13-15H,1-12H3
• Clave InChI: VKOLBYNBPONPAE-UHFFFAOYSA-N

Descripción

Aplicación

1,3,5-Phenyltriboronic acid, tris(pinacol) ester can undergo Suzuki–Miyaura cross-coupling polycondensation reaction with 4,7-dibromobenzo[c][1,2,5]thiadiazole to afford conjugated polybenzothiadiazoles. It may also be used as a crosslinker for synthesizing conjugated microporous polymer (CMP) nanoparticles. This product was previously listed as BML00299.

Otras notas

Molecular engineering of conjugated polybenzothiadiazoles for enhanced hydrogen production by photosynthesis

Conjugated microporous polymer nanoparticles with enhanced dispersibility and water compatibility for photocatalytic applications

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable