製品名:ethyl 5-(2,1,3-benzothiadiazole-5-amido)pyrazolo[1,5-a]pyridine-3-carboxylate

IUPAC Name:ethyl 5-(2,1,3-benzothiadiazole-5-amido)pyrazolo[1,5-a]pyridine-3-carboxylate

CAS番号:1396851-10-7
分子式:C17H13N5O3S
純度:95%+
カタログ番号:CM915608
分子量:367.38

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製品詳細

CAS番号:1396851-10-7
分子式:C17H13N5O3S
融点:-
SMILESコード:CCOC(=O)C1=C2C=C(NC(=O)C3=CC4=NSN=C4C=C3)C=CN2N=C1
密度:
カタログ番号:CM915608
分子量:367.38
沸点:
MDL番号:
保管方法:

Category Infos

Pyrazolopyridines
Over the past few years, many pyrazole fused-ring systems, especially with applications in medicinal chemistry, have been published. These include general structures such as pyrazoline, pyrazoline, pyrazoquinoline, pyrazoloisoquinoline, pyrazoline, pyrazolopyrazine, pyrazolopyrazine, pyranopyrazole, pyrano Pyrazoles, pyrazolotriazines and pyrazole fused phosphorus rings.
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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