Produktname:1-(2H-1,3-benzodioxole-5-carbonyl)-N-(2,1,3-benzothiadiazol-4-yl)azetidine-3-carboxamide
IUPAC Name:1-(2H-1,3-benzodioxole-5-carbonyl)-N-(2,1,3-benzothiadiazol-4-yl)azetidine-3-carboxamide
- CAS：1448069-30-4
- Molekulare Formel：C18H14N4O4S
- Reinheit：95%+
- Katalognummer：CM796186
- Molekulargewicht：382.39
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Produkt-Details
- CAS-Nr.:1448069-30-4
- Molekulare Formel:C18H14N4O4S
- Schmelzpunkt:-
- SMILES-Code:O=C(NC1=CC=CC2=NSN=C12)C1CN(C1)C(=O)C1=CC2=C(OCO2)C=C1
- Dichte:
- Katalognummer:CM796186
- Molekulargewicht:382.39
- Siedepunkt:
- Mdl-Nr.:
- Lagerung:
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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