Nom du produit:5-[3-(4-chlorobenzenesulfonyl)azetidine-1-carbonyl]-2,1,3-benzothiadiazole
IUPAC Name:5-[3-(4-chlorobenzenesulfonyl)azetidine-1-carbonyl]-2,1,3-benzothiadiazole
- CAS：1448073-31-1
- Formule moléculaire：C16H12ClN3O3S2
- Pureté：95%+
- Numéro de catalogue：CM899452
- Poids moléculaire：393.86
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Détails du produit
- N° CAS:1448073-31-1
- Formule moléculaire:C16H12ClN3O3S2
- Point de fusion:-
- Code SMILES:ClC1=CC=C(C=C1)S(=O)(=O)C1CN(C1)C(=O)C1=CC2=NSN=C2C=C1
- Densité:
- Numéro de catalogue:CM899452
- Poids moléculaire:393.86
- 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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