Название продукции:N-[5-(2,1,3-benzothiadiazole-5-carbonyl)-4H,5H,6H,7H-[1,3]thiazolo[5,4-c]pyridin-2-yl]cyclopropanecarboxamide

IUPAC Name:N-[5-(2,1,3-benzothiadiazole-5-carbonyl)-4H,5H,6H,7H-[1,3]thiazolo[5,4-c]pyridin-2-yl]cyclopropanecarboxamide

CAS:1351645-97-0
Молекулярная формула:C17H15N5O2S2
Чистота:95%+
Номер в каталоге:CM999545
Молекулярная масса:385.46

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Информация о продукции

Номер CAS:1351645-97-0
Молекулярная формула:C17H15N5O2S2
Точка плавления:-
Smiles-код:O=C(NC1=NC2=C(CN(CC2)C(=O)C2=CC3=NSN=C3C=C2)S1)C1CC1
Плотность:
Номер в каталоге:CM999545
Молекулярная масса:385.46
Точка кипения:
Номер Mdl:
Хранение:

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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