Nombre del producto:4,7-Dibromo-5,6-difluorobenzo[c][1,2,5]thiadiazole

IUPAC Name:4,7-dibromo-5,6-difluoro-2,1,3-benzothiadiazole

CAS:1295502-53-2
Fórmula molecular:C6Br2F2N2S
Pureza:95%+
Número de catálogo:CM157461
Peso molecular:329.94

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Detalles del producto

Núm. De CAS :1295502-53-2
Fórmula molecular:C6Br2F2N2S
Punto de fusión:-
Código de sonrisas:FC1=C(Br)C2=NSN=C2C(Br)=C1F
Densidad:
Número de catálogo:CM157461
Peso molecular:329.94
Punto de ebullición:318.2°C at 760 mmHg
Nº Mdl:
Almacenamiento:Store at room temperature.

Category Infos

Benzimidazoles
Benzimidazole is a benzo derivative of imidazole. It is a kind of bicyclic aromatic organic compounds, which is formed by fusing a six-membered benzene ring and five-membered imidazole at positions 4 and 5 of imidazole ring. It is an important pharmacophore of many biologically active heterocyclic compounds with various pharmacological activities. Benzimidazoles and their derivatives have developed into dynamic heterocyclic systems due to their potency in a variety of biologically active compounds such as anticancer, bactericidal and antiviral drugs. Benzimidazoles are a class of therapeutic motifs with broad relevance in medicinal chemistry.
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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