Nom du produit:N-(2,1,3-benzothiadiazol-4-yl)imidazo[1,2-b]pyridazine-6-carboxamide

IUPAC Name:N-(2,1,3-benzothiadiazol-4-yl)imidazo[1,2-b]pyridazine-6-carboxamide

CAS:2415464-44-5
Formule moléculaire:C13H8N6OS
Pureté:95%+
Numéro de catalogue:CM646339
Poids moléculaire:296.31

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Détails du produit

N° CAS:2415464-44-5
Formule moléculaire:C13H8N6OS
Point de fusion:-
Code SMILES:O=C(NC1=CC=CC2=NSN=C12)C1=NN2C=CN=C2C=C1
Densité:
Numéro de catalogue:CM646339
Poids moléculaire:296.31
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.
Imidazopyridazines
Potent IRAK-4 inhibitors have been reported by several groups including some structurally related benzimidazoles as well as alternative fused heterocycles such as the imidazopyridine and imidazopyridazine. Such compounds are reported to have IRAK-1 and IRAK-4 activity with varying degrees of selectivity.

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