製品名:Benzo[c][1,2,5]thiadiazol-4-ylboronic acid

IUPAC Name:(2,1,3-benzothiadiazol-4-yl)boronic acid

CAS番号:499769-94-7
分子式:C6H5BN2O2S
純度:95%
カタログ番号:CM214686
分子量:179.99

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CM214686-1g 1-2 Weeks ƥƥƥʼn

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製品詳細

CAS番号:499769-94-7
分子式:C6H5BN2O2S
融点:-
SMILESコード:OB(C1=CC=CC2=NSN=C21)O
密度:
カタログ番号:CM214686
分子量:179.99
沸点:
MDL番号:MFCD05664667
保管方法:

Category Infos

Boronic Acids and Esters
Boronic acids and boronate esters are commonly used reagents in Suzuki–Miyaura coupling chemistry. Organoboron derivatives are common reagents for C–C bond formation, either through classical palladium-mediated transformations or through other newer coupling methods. Boronic esters and acids are potential intermediates in the manufacture of many active pharmaceutical ingredients (API).
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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.