900989

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

≥97%

• Synonym(e): 1,3,5-Tris(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene
• Empirische Formel (Hill-System): C₂₄H₃₉B₃O₆
• CAS-Nummer: 365564-05-2
• Molekulargewicht: 456.00
• MDL-Nummer: MFCD17167305
• UNSPSC-Code: 12352106
• NACRES: NA.06

Eigenschaften

• Qualitätsniveau: 100
• Assay: ≥97%
• Form: powder or crystals
• mp (Schmelzpunkt): 286-287 °C
• SMILES String: 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
• InChIKey: VKOLBYNBPONPAE-UHFFFAOYSA-N

Beschreibung

Anwendung

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.

Sonstige Hinweise

Molecular engineering of conjugated polybenzothiadiazoles for enhanced hydrogen production by photosynthesis

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

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable