Nom du produit:N-(2,1,3-benzothiadiazol-4-yl)-1-(3,4-difluorobenzoyl)azetidine-3-carboxamide
IUPAC Name:N-(2,1,3-benzothiadiazol-4-yl)-1-(3,4-difluorobenzoyl)azetidine-3-carboxamide
- CAS：1448051-47-5
- Formule moléculaire：C17H12F2N4O2S
- Pureté：95%+
- Numéro de catalogue：CM938773
- Poids moléculaire：374.37
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Détails du produit
- N° CAS:1448051-47-5
- Formule moléculaire:C17H12F2N4O2S
- Point de fusion:-
- Code SMILES:FC1=C(F)C=C(C=C1)C(=O)N1CC(C1)C(=O)NC1=CC=CC2=NSN=C12
- Densité:
- Numéro de catalogue:CM938773
- Poids moléculaire:374.37
- Point d'ébullition:
- N° Mdl:
- Stockage:
Category Infos
- 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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