Nom du produit:5-[3-(3-phenyl-1,2,4-oxadiazol-5-yl)azetidine-1-carbonyl]-2,1,3-benzothiadiazole

IUPAC Name:5-[3-(3-phenyl-1,2,4-oxadiazol-5-yl)azetidine-1-carbonyl]-2,1,3-benzothiadiazole

CAS:1251681-19-2
Formule moléculaire:C18H13N5O2S
Pureté:95%+
Numéro de catalogue:CM903680
Poids moléculaire:363.4

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Détails du produit

N° CAS:1251681-19-2
Formule moléculaire:C18H13N5O2S
Point de fusion:-
Code SMILES:O=C(N1CC(C1)C1=NC(=NO1)C1=CC=CC=C1)C1=CC2=NSN=C2C=C1
Densité:
Numéro de catalogue:CM903680
Poids moléculaire:363.4
Point d'ébullition:
N° Mdl:
Stockage:

Category Infos

Oxadiazoles
Oxadiazoles are a class of heterocyclic aromatic compounds with the molecular formula C2H2N2O, which have special biological activities and thermodynamic properties. Five-membered heterocyclic moieties composed of three or two heteroatoms are of great interest to researchers because these compounds show significant therapeutic potential. These heterocycles can serve as a building block for the development of novel molecular structures.
Azetidines
Azetidines are an important class of saturated four-membered nitrogen-containing heterocyclic compounds. The research hotspots related to this structure mainly focus on two aspects: one is the research of pharmaceutical chemistry; the other is related to chiral azetidines, using rigid azetidine compounds as chiral ligands for asymmetric catalytic reactions. Many nitrogen-containing heterocycles play important roles in drug structures, and in many cases small structural changes can improve ligand selectivity and pharmacokinetic properties.
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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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