Nom du produit:5,6-Difluoro-4,7-di(thiophen-2-yl)benzo[c][1,2,5]thiadiazole
IUPAC Name:5,6-difluoro-4,7-bis(thiophen-2-yl)-2,1,3-benzothiadiazole
- CAS：1304773-88-3
- Formule moléculaire：C14H6F2N2S3
- Pureté：97%
- Numéro de catalogue：CM493243
- Poids moléculaire：336.39
Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:1304773-88-3
- Formule moléculaire:C14H6F2N2S3
- Point de fusion:-
- Code SMILES:FC1=C(C2=CC=CS2)C3=NSN=C3C(C4=CC=CS4)=C1F
- Densité:
- Numéro de catalogue:CM493243
- Poids moléculaire:336.39
- Point d'ébullition:
- N° Mdl:
- Stockage:Keep in dark place,Sealed in dry,Room Temperature
Category Infos
- Thiophenes
- Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.
- 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.
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