13399-12-7

Basic information

• Product Name: Benzo[1,2-d:4,5-d]bisthiazole, 2,6-dimethyl- (6CI,7CI,8CI,9CI)
• Synonyms: Benzo[1,2-d:4,5-d]bisthiazole, 2,6-dimethyl- (6CI,7CI,8CI,9CI);5,11-Dimethyl-4,10-dithia-6,12- diazatricyclo-[7.3.0.0^{3,7}]dodeca-1,3(7),5,8,11-pentaene;2,6-Dimethylbenzo[1,2-d:4,5-d']bis[1,3]thiazole
• CAS NO: 13399-12-7
• Molecular Formula: C10H8N2S2
• Molecular Weight: 220.31392
• Product Categories: BENZOTHIAZOLE
• Mol File: 13399-12-7.mol
• Article Data: 3

Chemical Properties

• Melting Point: 100 °C
• Boiling Point: 368.1±15.0 °C(Predicted)
• Appearance: /
• Density: 1.415±0.06 g/cm3(Predicted)
• PKA: -0.34±0.50(Predicted)
• CAS DataBase Reference: Benzo[1,2-d:4,5-d]bisthiazole, 2,6-dimethyl- (6CI,7CI,8CI,9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Benzo[1,2-d:4,5-d]bisthiazole, 2,6-dimethyl- (6CI,7CI,8CI,9CI)(13399-12-7)
• EPA Substance Registry System: Benzo[1,2-d:4,5-d]bisthiazole, 2,6-dimethyl- (6CI,7CI,8CI,9CI)(13399-12-7)

Safety Data

• Hazardous Substances Data: 13399-12-7(Hazardous Substances Data)

Upstream product

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

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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

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.