Nombre del producto:N-(5-cyano-1,3-thiazol-2-yl)-2,1,3-benzothiadiazole-5-carboxamide

IUPAC Name:N-(5-cyano-1,3-thiazol-2-yl)-2,1,3-benzothiadiazole-5-carboxamide

CAS:1251614-09-1
Fórmula molecular:C11H5N5OS2
Pureza:95%+
Número de catálogo:CM969826
Peso molecular:287.32

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Detalles del producto

Núm. De CAS :1251614-09-1
Fórmula molecular:C11H5N5OS2
Punto de fusión:-
Código de sonrisas:O=C(NC1=NC=C(S1)C#N)C1=CC2=NSN=C2C=C1
Densidad:
Número de catálogo:CM969826
Peso molecular:287.32
Punto de ebullición:
Nº Mdl:
Almacenamiento:

Category Infos

Thiazoles
Thiazoles are very important functional groups in medicinal chemistry. They act as ligands on a variety of biological matrices. Thiazoles are used in a wide range of therapeutic applications, such as antibacterial, antiretroviral, antifungal, antiallergic, antihypertensive, pain treatment, and to control symptoms of schizophrenia.
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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