cas 2035036-12-3|| where to buy (2E)-3-(2-chlorophenyl)-N-(1,3,6-trimethyl-2,2-dioxo-1,3-dihydro-2lambda6,1,3-benzothiadiazol-5-yl)prop-2-enamide

製品名:(2E)-3-(2-chlorophenyl)-N-(1,3,6-trimethyl-2,2-dioxo-1,3-dihydro-2lambda6,1,3-benzothiadiazol-5-yl)prop-2-enamide

IUPAC Name:(2E)-3-(2-chlorophenyl)-N-(1,3,6-trimethyl-2,2-dioxo-1,3-dihydro-2λ⁶,1,3-benzothiadiazol-5-yl)prop-2-enamide

: CAS番号：2035036-12-3; 分子式：C18H18ClN3O3S; 純度：95%+

: カタログ番号：CM773701; 分子量：391.87

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製品詳細

: CAS番号:2035036-12-3; 分子式:C18H18ClN3O3S; 融点:-; SMILESコード:CN1C2=C(C=C(NC(=O)\C=C\C3=C(Cl)C=CC=C3)C(C)=C2)N(C)S1(=O)=O; 密度:

: カタログ番号:CM773701; 分子量:391.87; 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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