Nom du produit:N-(2-{[3-(4-fluorophenyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]oxy}ethyl)-2,1,3-benzothiadiazole-5-carboxamide

IUPAC Name:N-(2-{[3-(4-fluorophenyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]oxy}ethyl)-2,1,3-benzothiadiazole-5-carboxamide

CAS:1203022-76-7
Formule moléculaire:C20H14FN7O2S
Pureté:95%+
Numéro de catalogue:CM939259
Poids moléculaire:435.44

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Détails du produit

N° CAS:1203022-76-7
Formule moléculaire:C20H14FN7O2S
Point de fusion:-
Code SMILES:FC1=CC=C(C=C1)C1=NN=C2C=CC(OCCNC(=O)C3=CC4=NSN=C4C=C3)=NN12
Densité:
Numéro de catalogue:CM939259
Poids moléculaire:435.44
Point d'ébullition:
N° Mdl:
Stockage:

Category Infos

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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