cas 1421500-50-6|| where to buy N-(2,1,3-benzothiadiazol-4-yl)-2-(thiophene-3-amido)-1,3-oxazole-4-carboxamide

Название продукции:N-(2,1,3-benzothiadiazol-4-yl)-2-(thiophene-3-amido)-1,3-oxazole-4-carboxamide

IUPAC Name:N-(2,1,3-benzothiadiazol-4-yl)-2-(thiophene-3-amido)-1,3-oxazole-4-carboxamide

: CAS：1421500-50-6; Молекулярная формула：C15H9N5O3S2; Чистота：95%+

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: Номер CAS:1421500-50-6; Молекулярная формула:C15H9N5O3S2; Точка плавления:-; Smiles-код:O=C(NC1=NC(=CO1)C(=O)NC1=CC=CC2=NSN=C12)C1=CSC=C1; Плотность:

: Номер в каталоге:CM940107; Молекулярная масса:371.39; Точка кипения:; Номер Mdl:; Хранение:

: 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.

: Oxazoles; Oxazoles are heterocyclic aromatic compounds containing one oxygen atom and one nitrogen atom, separated by a carbon atom. The presence of two heteroatoms (oxygen and nitrogen) provides possible interactions (hydrogen, hydrophobic, van der Waals or dipole bonds) with a wide range of receptors and enzymes. Oxazole rings are valuable heterocyclic scaffolds for the design of novel therapeutics with anticancer, antiviral, antibacterial, anti-inflammatory, neuroprotective, antidiabetic, and antidepressant properties due to their wide range of targets and biological activities.

: 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.