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Product Name:4,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,1,3-benzothiadiazole
CAS:934365-16-9
Purity:98% Package:10g;100g;500g;1kg;5kg;10kg,100kg,1ton Remarks:OLED
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| | 4,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,1,3-benzothiadiazole Basic information |
| Product Name: | 4,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,1,3-benzothiadiazole | | Synonyms: | 4,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,1,3-benzothiadiazole;2,1,3-Benzothiadiazole-4,7-diboronic Acid Bis(pinacol) Ester;2,1,3-Benzothiadiazole-4,7-diboronic acid, pinacol ester;2,1,3-Benzothiadiazole-4,7-diboronic acid, pinacol ester 98%;2,1,3-Benzothiadiazole-4,7-bis(pinacolato)diboronic ester;2,1,3-Benzothiadiazole, 4,7-bis(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-;bis(3-hydroxy-2,3-dimethylbutan-2-yl) benzo[c][1,2,5]thiadiazole-4,7-diylbis(hydrogen boronate);4,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) | | CAS: | 934365-16-9 | | MF: | C18H26B2N2O4S | | MW: | 388.1 | | EINECS: | | | Product Categories: | | | Mol File: | 934365-16-9.mol |  |
| | 4,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,1,3-benzothiadiazole Chemical Properties |
| Melting point | 208.5-209.5℃ (hexane ) | | Boiling point | 482.6±30.0 °C(Predicted) | | density | 1.18±0.1 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | form | powder | | pka | 0.67±0.50(Predicted) | | color | White/Off-white | | InChI | InChI=1S/C18H26B2N2O4S/c1-15(2)16(3,4)24-19(23-15)11-9-10-12(14-13(11)21-27-22-14)20-25-17(5,6)18(7,8)26-20/h9-10H,1-8H3 | | InChIKey | DHWADSHFLSDMBJ-UHFFFAOYSA-N | | SMILES | N1=C2C(B3OC(C)(C)C(C)(C)O3)=CC=C(B3OC(C)(C)C(C)(C)O3)C2=NS1 |
| Safety Statements | 24/25 | | WGK Germany | 3 | | HS Code | 29349990 | | Storage Class | 11 - Combustible Solids |
| | 4,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,1,3-benzothiadiazole Usage And Synthesis |
| Description | 4,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,1,3-benzothiadiazole is a benzothiadiazole based donor–acceptor, which can be used in photodiode devices.[1] | | References | [1] SHARMA B, SAROTHIA Y, SINGH R, et al. Synthesis and characterization of light-absorbing cyclopentadithiophene-based donor–acceptor copolymers[J]. Polymer International, 2016, 65: 57-65. DOI:10.1002/PI.5024. |
| | 4,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,1,3-benzothiadiazole Preparation Products And Raw materials |
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