Название продукции:N-{[5-(thiophene-2-carbonyl)thiophen-2-yl]methyl}-2,1,3-benzothiadiazole-5-carboxamide
IUPAC Name:N-{[5-(thiophene-2-carbonyl)thiophen-2-yl]methyl}-2,1,3-benzothiadiazole-5-carboxamide
- CAS：1421441-71-5
- Молекулярная формула：C17H11N3O2S3
- Чистота：95%+
- Номер в каталоге：CM999806
- Молекулярная масса：385.47
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Информация о продукции
- Номер CAS:1421441-71-5
- Молекулярная формула:C17H11N3O2S3
- Точка плавления:-
- Smiles-код:O=C(NCC1=CC=C(S1)C(=O)C1=CC=CS1)C1=CC2=NSN=C2C=C1
- Плотность:
- Номер в каталоге:CM999806
- Молекулярная масса:385.47
- Точка кипения:
- Номер Mdl:
- Хранение:
Category Infos
- Thiophenes
- Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.
- 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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