Nom du produit:N-(2,1,3-benzothiadiazol-4-yl)-2-[3-(4-methylphenyl)-6-oxo-1,6-dihydropyridazin-1-yl]propanamide

IUPAC Name:N-(2,1,3-benzothiadiazol-4-yl)-2-[3-(4-methylphenyl)-6-oxo-1,6-dihydropyridazin-1-yl]propanamide

CAS:1226444-68-3
Formule moléculaire:C20H17N5O2S
Pureté:95%+
Numéro de catalogue:CM638907
Poids moléculaire:391.45

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Détails du produit

N° CAS:1226444-68-3
Formule moléculaire:C20H17N5O2S
Point de fusion:-
Code SMILES:CC(N1N=C(C=CC1=O)C1=CC=C(C)C=C1)C(=O)NC1=CC=CC2=NSN=C12
Densité:
Numéro de catalogue:CM638907
Poids moléculaire:391.45
Point d'ébullition:
N° Mdl:
Stockage:

Category Infos

Pyridazines
Pyridazine, also known as o-diazobenzene, is a six-membered heterocyclic compound containing two nitrogen heteroatoms in the 1 and 2 positions with a special structure and a wide biological activity. Pyridazine is more and more popular in drug development, and a variety of pyridazine drugs have been developed and marketed. From the perspective of the therapeutic field, pyridazine drug molecules are mainly used for tumor treatment, but also involve in many therapeutic fields such as inflammation, hypertension and cardiovascular disease. With the increase and in-depth of research, pyridazine drugs will play more roles in the treatment of diseases.
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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