Nom du produit:Benzo[c][1,2,5]thiadiazol-4-ylboronic acid
IUPAC Name:(2,1,3-benzothiadiazol-4-yl)boronic acid
- CAS:499769-94-7
- Formule moléculaire:C6H5BN2O2S
- Pureté:95%
- Numéro de catalogue:CM214686
- Poids moléculaire:179.99
Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:499769-94-7
- Formule moléculaire:C6H5BN2O2S
- Point de fusion:-
- Code SMILES:OB(C1=CC=CC2=NSN=C21)O
- Densité:
- Numéro de catalogue:CM214686
- Poids moléculaire:179.99
- Point d'ébullition:
- N° Mdl:MFCD05664667
- Stockage:
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.