| Identification | Back Directory | [Name]
4,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,1,3-benzothiadiazole | [CAS]
934365-16-9 | [Synonyms]
BT-2B
4,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)
2,1,3-Benzothiadiazole-4,7-diboronic acid, pinacol ester
2,1,3-Benzothiadiazole-4,7-bis(pinacolato)diboronic ester
2,1,3-Benzothiadiazole-4,7-diboronic acid, pinacol ester 98%
2,1,3-Benzothiadiazole-4,7-diboronic Acid Bis(pinacol) Ester
2,1,3-Benzothiadiazole-4,7-Bis(Boronic Acid Pinacol Ester),>98%
4,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,1,3-benzothiadiazole
2,1,3-Benzothiadiazole, 4,7-bis(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-
4,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,1,3-benzothiadiazole >
bis(3-hydroxy-2,3-dimethylbutan-2-yl) benzo[c][1,2,5]thiadiazole-4,7-diylbis(hydrogen boronate) | [Molecular Formula]
C18H26B2N2O4S | [MDL Number]
MFCD11656086 | [MOL File]
934365-16-9.mol | [Molecular Weight]
388.097 |
| Chemical Properties | Back Directory | [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 | [Description]
2,1,3-Benzothiadiazole-4,7-bis(boronic acid pinacol ester) is an intermediate for the synthesis of small molecules, oligomers and polymers?via Suzuki Coupling reactions. Those small molecules, oligmomers and polymers can be?printed, spray-coated or?spin-coated?onto devices for?Organic Light-Emitting Diodes (OLED/PLED), Organic Field-Effect Transistors and Organic Photovoltaic devices. | [Odor]
White/Off-white powder |
| Hazard Information | Back Directory | [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. |
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