13399-12-7

Upstream product

• 3796-77-8 N-(2-methyl-1,3-benzothiazol-6-yl)thioacetamide 
• 10374-64-8 N,N'-p-phenylene-bis-thioacetamide 
• 43036-83-5 2,5-bis-sulfosulfanyl-benzene-1,4-diamine 
• 108-24-7 acetic anhydride 
• 101420-68-2 2-methyl-6-nitro-benzothiazol-5-ylamine 
• 13242-98-3 (6-isothiocyanato-benzothiazol-2-yl)-malonic acid diethyl ester 
• 13242-99-4 6-isothiocyanato-2-methyl-benzothiazole 
• 78-39-7 Triethyl orthoacetate 
• 75464-52-7 2,5-diaminobenzene-1,4-dithiol bis(hydrochloride) 
• 10386-10-4 [(4-isothiocyanato-phenyl)-thiocarbamoyl]-malonic acid diethyl ester 
• 68867-19-6 N-(2-methyl-1,3-benzothiazol-6-yl)acetamide 

Downstream Products

• 1421698-01-2 C₃₀H₂₄N₃S₂⁽¹⁺⁾*I^(1-) 
• 1421698-03-4 C₂₃H₂₅N₄S₂⁽¹⁺⁾*I^(1-) 
• 1421698-04-5 C₂₂H₂₄N₃O₂S₂⁽¹⁺⁾*I^(1-) 
• 1421698-05-6 C₂₄H₂₈N₃O₂S₂⁽¹⁺⁾*I^(1-) 
• 1421698-06-7 C₂₂H₂₂N₃S₂⁽¹⁺⁾*I^(1-) 
• 1421698-00-1 C₂₀H₂₀N₃S₂⁽¹⁺⁾*I^(1-) 

Relevant academic research and scientific papers

Quadrupolar benzobisthiazole-cored arylamines as highly efficient two-photon absorbing fluorophores

A computer-aided design of novel D-π-A-π-D styrylamines containing five isomeric benzobisthiazole moieties as the electron-accepting core has revealed the linear centrosymmetric benzo[1,2-d:4,5-d′]bisthiazole as the most promising building block for engin

Conjugated push-pull salts derived from linear benzobisthiazole: Preparation and optical properties

A series of novel monomethylated salts derived from linear benzobisthiazole was prepared. The push-pull attributes of these new compounds are represented by a quaternised azolium cycle as the acceptor part at one end of the structure and the dialkylamino- or diarylamino-substituted benzene ring as the donor part at the opposite end. Both moieties are connected by a conjugated linker consisting of one or two double bonds. Such dipolar structures are promising candidates for non-linear optical materials. The quantum-chemical indices describing linear and non-linear optical properties were obtained from semi-empirical calculations. The relationships between the chemical structure and non-linear optical properties of the cations studied were obtained. Effective conjugation was confirmed by measuring the optical properties in the UV-VIS region.

Facile synthesis of 2,6-disubstituted benzobisthiazoles: Functional monomers for the design of organic semiconductors

(Chemical Equation Presented) The synthesis of several synthetically useful 2,6-disubstituted benzobisthiazoles is described. The method is based on the Lewis acid-catalyzed ring-closing reaction between substituted orthoesters and diamino benzene dithiol. The resulting benzobisthiazoles are obtained cleanly and in good yields. These materials are of interest for the development of new organic semiconductors.