Nom du produit:ethyl 5-(2,1,3-benzothiadiazole-5-amido)pyrazolo[1,5-a]pyridine-3-carboxylate

IUPAC Name:ethyl 5-(2,1,3-benzothiadiazole-5-amido)pyrazolo[1,5-a]pyridine-3-carboxylate

CAS:1396851-10-7
Formule moléculaire:C17H13N5O3S
Pureté:95%+
Numéro de catalogue:CM915608
Poids moléculaire:367.38

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Détails du produit

N° CAS:1396851-10-7
Formule moléculaire:C17H13N5O3S
Point de fusion:-
Code SMILES:CCOC(=O)C1=C2C=C(NC(=O)C3=CC4=NSN=C4C=C3)C=CN2N=C1
Densité:
Numéro de catalogue:CM915608
Poids moléculaire:367.38
Point d'ébullition:
N° Mdl:
Stockage:

Category Infos

Pyrazolopyridines
Over the past few years, many pyrazole fused-ring systems, especially with applications in medicinal chemistry, have been published. These include general structures such as pyrazoline, pyrazoline, pyrazoquinoline, pyrazoloisoquinoline, pyrazoline, pyrazolopyrazine, pyrazolopyrazine, pyranopyrazole, pyrano Pyrazoles, pyrazolotriazines and pyrazole fused phosphorus rings.
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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