Название продукции:N-(2,1,3-benzothiadiazol-4-yl)-2-{2-[(2-oxo-2-phenylethyl)sulfanyl]-1,3-thiazol-4-yl}acetamide
IUPAC Name:N-(2,1,3-benzothiadiazol-4-yl)-2-{2-[(2-oxo-2-phenylethyl)sulfanyl]-1,3-thiazol-4-yl}acetamide
- CAS：1207037-73-7
- Молекулярная формула：C19H14N4O2S3
- Чистота：95%+
- Номер в каталоге：CM939735
- Молекулярная масса：426.53
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Информация о продукции
- Номер CAS:1207037-73-7
- Молекулярная формула:C19H14N4O2S3
- Точка плавления:-
- Smiles-код:O=C(CC1=CSC(SCC(=O)C2=CC=CC=C2)=N1)NC1=CC=CC2=NSN=C12
- Плотность:
- Номер в каталоге:CM939735
- Молекулярная масса:426.53
- Точка кипения:
- Номер Mdl:
- Хранение:
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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