cas 1428351-84-1|| where to buy N-({4-oxo-3-[2-(pyrrolidin-1-yl)ethyl]-3,4-dihydrophthalazin-1-yl}methyl)-2,1,3-benzothiadiazole-5-carboxamide

Nombre del producto: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; Fórmula molecular：C22H22N6O2S; Pureza：95%+

: Número de catálogo：CM930346; Peso molecular：434.52

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Detalles del producto

: Núm. De CAS :1428351-84-1; Fórmula molecular:C22H22N6O2S; Punto de fusión:-; Código de sonrisas:O=C(NCC1=NN(CCN2CCCC2)C(=O)C2=C1C=CC=C2)C1=CC2=NSN=C2C=C1; Densidad:

: Número de catálogo:CM930346; Peso molecular:434.52; Punto de ebullición:; Nº Mdl:; Almacenamiento:

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.

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