Nom du produit:4-(2,1,3-benzothiadiazol-5-yl)-N-(2-methoxyphenyl)-1,3-thiazol-2-amine hydrochloride
IUPAC Name:4-(2,1,3-benzothiadiazol-5-yl)-N-(2-methoxyphenyl)-1,3-thiazol-2-amine hydrochloride
- CAS：2034250-46-7
- Formule moléculaire：C16H13ClN4OS2
- Pureté：95%+
- Numéro de catalogue：CM686446
- Poids moléculaire：376.88
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Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:2034250-46-7
- Formule moléculaire:C16H13ClN4OS2
- Point de fusion:-
- Code SMILES:Cl.COC1=C(NC2=NC(=CS2)C2=CC3=NSN=C3C=C2)C=CC=C1
- Densité:
- Numéro de catalogue:CM686446
- Poids moléculaire:376.88
- Point d'ébullition:
- N° Mdl:
- Stockage:
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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