cas 2034483-13-9|| where to buy 2-(4-chlorophenoxy)-N-(1,3-dimethyl-2,2-dioxo-1,3-dihydro-2lambda6,1,3-benzothiadiazol-5-yl)-2-methylpropanamide

製品名:2-(4-chlorophenoxy)-N-(1,3-dimethyl-2,2-dioxo-1,3-dihydro-2lambda6,1,3-benzothiadiazol-5-yl)-2-methylpropanamide

IUPAC Name:2-(4-chlorophenoxy)-N-(1,3-dimethyl-2,2-dioxo-1,3-dihydro-2λ⁶,1,3-benzothiadiazol-5-yl)-2-methylpropanamide

: CAS番号：2034483-13-9; 分子式：C18H20ClN3O4S; 純度：95%+

: カタログ番号：CM821541; 分子量：409.89

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製品詳細

: CAS番号:2034483-13-9; 分子式:C18H20ClN3O4S; 融点:-; SMILESコード:CN1C2=C(C=C(NC(=O)C(C)(C)OC3=CC=C(Cl)C=C3)C=C2)N(C)S1(=O)=O; 密度:

: カタログ番号:CM821541; 分子量:409.89; 沸点:; MDL番号:; 保管方法:

Category Infos

: 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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