Nom du produit:3-{[1-(2,1,3-benzothiadiazole-5-carbonyl)piperidin-4-yl]methyl}-4-(2-fluorophenyl)-4,5-dihydro-1H-1,2,4-triazol-5-one

IUPAC Name:3-{[1-(2,1,3-benzothiadiazole-5-carbonyl)piperidin-4-yl]methyl}-4-(2-fluorophenyl)-4,5-dihydro-1H-1,2,4-triazol-5-one

CAS:2034584-33-1
Formule moléculaire:C21H19FN6O2S
Pureté:95%+
Numéro de catalogue:CM872891
Poids moléculaire:438.48

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Détails du produit

N° CAS:2034584-33-1
Formule moléculaire:C21H19FN6O2S
Point de fusion:-
Code SMILES:FC1=C(C=CC=C1)N1C(=O)NN=C1CC1CCN(CC1)C(=O)C1=CC2=NSN=C2C=C1
Densité:
Numéro de catalogue:CM872891
Poids moléculaire:438.48
Point d'ébullition:
N° Mdl:
Stockage:

Category Infos

Piperidines
Piperidine is an azacycloalkane that is cyclohexane in which one of the carbons is replaced by a nitrogen. Although piperidine is a common organic compound, it is an immensely important class of compounds medicinally: the piperidine ring is the most common heterocyclic subunit among FDA approved drugs.
Piperidine,Piperidine Price
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Triazoles
Triazole refers to a heterocyclic compound with the molecular formula C2H3N3, which has a five-membered ring consisting of two carbon atoms and three nitrogen atoms. Neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease already affect many people around the world, and these numbers are increasing rapidly. Treatment for these disorders is often aimed at relieving symptoms and has no cure. Research on new molecules is underway, and heterocyclic compounds have important pharmacological implications. Triazoles and tetrazoles are emerging as new molecules in this field.
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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