製品名:1-methyl-1H-1,3-benzodiazol-5-yl 2,1,3-benzothiadiazole-5-carboxylate

IUPAC Name:1-methyl-1H-1,3-benzodiazol-5-yl 2,1,3-benzothiadiazole-5-carboxylate

CAS番号:1351591-25-7
分子式:C15H10N4O2S
純度:95%+
カタログ番号:CM811845
分子量:310.33

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製品詳細

CAS番号:1351591-25-7
分子式:C15H10N4O2S
融点:-
SMILESコード:CN1C=NC2=C1C=CC(OC(=O)C1=CC3=NSN=C3C=C1)=C2
密度:
カタログ番号:CM811845
分子量:310.33
沸点:
MDL番号:
保管方法:

Category Infos

Benzimidazoles
Benzimidazole is a benzo derivative of imidazole. It is a kind of bicyclic aromatic organic compounds, which is formed by fusing a six-membered benzene ring and five-membered imidazole at positions 4 and 5 of imidazole ring. It is an important pharmacophore of many biologically active heterocyclic compounds with various pharmacological activities. Benzimidazoles and their derivatives have developed into dynamic heterocyclic systems due to their potency in a variety of biologically active compounds such as anticancer, bactericidal and antiviral drugs. Benzimidazoles are a class of therapeutic motifs with broad relevance in medicinal chemistry.
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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