Produktname:2-[(4-{[(2,1,3-benzothiadiazol-4-yl)carbamoyl]methyl}-1,3-thiazol-2-yl)sulfanyl]-N-(4-fluorophenyl)acetamide
IUPAC Name:2-[(4-{[(2,1,3-benzothiadiazol-4-yl)carbamoyl]methyl}-1,3-thiazol-2-yl)sulfanyl]-N-(4-fluorophenyl)acetamide
- CAS：1203086-23-0
- Molekulare Formel：C19H14FN5O2S3
- Reinheit：95%+
- Katalognummer：CM834855
- Molekulargewicht：459.53
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Produkt-Details
- CAS-Nr.:1203086-23-0
- Molekulare Formel:C19H14FN5O2S3
- Schmelzpunkt:-
- SMILES-Code:FC1=CC=C(NC(=O)CSC2=NC(CC(=O)NC3=CC=CC4=NSN=C34)=CS2)C=C1
- Dichte:
- Katalognummer:CM834855
- Molekulargewicht:459.53
- Siedepunkt:
- Mdl-Nr.:
- Lagerung:
Category Infos
- Thiazoles
- Thiazoles are very important functional groups in medicinal chemistry. They act as ligands on a variety of biological matrices. Thiazoles are used in a wide range of therapeutic applications, such as antibacterial, antiretroviral, antifungal, antiallergic, antihypertensive, pain treatment, and to control symptoms of schizophrenia.
- 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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