Produktname:2,1,3-Benzothiadiazole-4,7-diboronic acid
IUPAC Name:[7-(dihydroxyboranyl)-2,1,3-benzothiadiazol-4-yl]boronic acid
- CAS:1332458-85-1
- Molekulare Formel:C6H6B2N2O4S
- Reinheit:98%+
- Katalognummer:CM563527
- Molekulargewicht:223.8
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Produkt-Details
- CAS-Nr.:1332458-85-1
- Molekulare Formel:C6H6B2N2O4S
- Schmelzpunkt:-
- SMILES-Code:OB(C1=CC=C(B(O)O)C2=NSN=C21)O
- Dichte:
- Katalognummer:CM563527
- Molekulargewicht:223.8
- Siedepunkt:
- Mdl-Nr.:
- Lagerung:
Category Infos
- 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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- Benzothiadiazoles
- The two N atoms in Benzothiadiazole could possibly form intermolecular hydrogen bonding, leading to a more planar backbone. Benzothiadiazole is a strong electron-accepting molecular fragment. By fusing it with thiazole donor-acceptor dyes, near-infrared fluorescence was created. The benzothiadiazole ring is a useful n-type building block for designing electron-transport materials for organic and polymer light-emitting diodes (LEDs). Arene- and heteroarene-fused thiadiazoles have also found use in the design of low-band-gap materials for the construction of organic field-effect transmitters (OFETs), as stable organic radicals, and as one or two photon-absorbing materials for the design of nonlinear near-infrared (NIR) dyes. Benzothiadiazoles acting as the electron-accepting cores have been incorporated into dendrimer-type light-harvesting materials.