Produktname:1,2-Bis(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethane

IUPAC Name:4,4,5,5-tetramethyl-2-(4-{2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]ethoxy}phenyl)-1,3,2-dioxaborolane

CAS:957061-07-3
Molekulare Formel:C26H36B2O6
Reinheit:97%
Katalognummer:CM219467
Molekulargewicht:466.18

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Produkt-Details

CAS-Nr.:957061-07-3
Molekulare Formel:C26H36B2O6
Schmelzpunkt:-
SMILES-Code:CC1(C)C(C)(C)OB(C2=CC=C(OCCOC3=CC=C(B4OC(C)(C)C(C)(C)O4)C=C3)C=C2)O1
Dichte:
Katalognummer:CM219467
Molekulargewicht:466.18
Siedepunkt:-
Mdl-Nr.:MFCD09258655
Lagerung:

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Boronic Acids and Esters
Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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The most common type of organic photodetector is the organic photodiode (OPD). The photodiode has a simple structure in which an active layer is sandwiched between a transparent electrode and a metal electrode. In contrast to OLEDs, organic photodiodes (OPDs) utilize the organic semiconductor to absorb incident light and convert it to electric current. The structure and working principle are more like organic solar cells. Among the various organic photodetectors, organic photodiodes (OPDs) have been the most widely studied due to their fast response, high sensitivity, and full use of the existing research base of organic photovoltaics (OPVs).