Nom du produit:5-(3-phenylazepane-1-carbonyl)-2,1,3-benzothiadiazole
IUPAC Name:5-(3-phenylazepane-1-carbonyl)-2,1,3-benzothiadiazole
- CAS：1706069-90-0
- Formule moléculaire：C19H19N3OS
- Pureté：95%+
- Numéro de catalogue：CM893754
- Poids moléculaire：337.44
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Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:1706069-90-0
- Formule moléculaire:C19H19N3OS
- Point de fusion:-
- Code SMILES:O=C(N1CCCCC(C1)C1=CC=CC=C1)C1=CC2=NSN=C2C=C1
- Densité:
- Numéro de catalogue:CM893754
- Poids moléculaire:337.44
- Point d'ébullition:
- N° Mdl:
- Stockage:
Category Infos
- Azepanes
- The use of azepane as a scaffold for drug discovery remains of interest. The azepane linker is the key to efficient activity. A number of seven-membered ring derivatives have been prepared or investigated for their potential or actual pharmacological properties. Examples include azaalkane derivatives as PKB (protein kinase B) inhibitors.
- 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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