Nom du produit:N-({4-oxo-3-[2-(pyrrolidin-1-yl)ethyl]-3,4-dihydrophthalazin-1-yl}methyl)-2,1,3-benzothiadiazole-5-carboxamide
IUPAC Name:N-({4-oxo-3-[2-(pyrrolidin-1-yl)ethyl]-3,4-dihydrophthalazin-1-yl}methyl)-2,1,3-benzothiadiazole-5-carboxamide
- CAS:1428351-84-1
- Formule moléculaire:C22H22N6O2S
- Pureté:95%+
- Numéro de catalogue:CM930346
- Poids moléculaire:434.52
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Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:1428351-84-1
- Formule moléculaire:C22H22N6O2S
- Point de fusion:-
- Code SMILES:O=C(NCC1=NN(CCN2CCCC2)C(=O)C2=C1C=CC=C2)C1=CC2=NSN=C2C=C1
- Densité:
- Numéro de catalogue:CM930346
- Poids moléculaire:434.52
- Point d'ébullition:
- N° Mdl:
- Stockage:
Category Infos
- Pyrrolidines
- Pyrrolidine, also known as tetrahydropyrrole, is a saturated five-membered heterocyclic ring, which is miscible with water. Pyrrolidine exists in many alkaloids and drug molecules, such as kappa opioids, antagonists of dopamine D4 receptors, and HIV reverse transcriptase inhibitors.
- Phthalazines
- Phthalazine is a heterocyclic compound with the molecular formula C8H6N2 composed of a benzene ring fused with a pyridazine ring. Phthalazine and its derivatives do not exist in nature. Phthalazines are used as starting materials for organic synthesis. Studies have found that phthalazine has a variety of physiological activities, such as anti-cancer, antibacterial, anti-inflammatory and so on. The synthesis of phthalazine compounds with novel structures and better biological activities has become a research hotspot in recent years.
- 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.