Identification | Back Directory | [Name]
5'-HEXYL-2,2'-BITHIOPHENE-5-BORONIC ACID PINACOL ESTER | [CAS]
579503-59-6 | [Synonyms]
5'-HEXYL-2,2'-BITHIOPHENE-5-BORONIC ACID PINACOL E 5'-n-hexyl-2,2'-bithiophene-5-boronic acid pinacol ester 5'-Hexyl-2,2'-bithiophene-5-boronic acid pinacol ester 97% 5'-HEXYL-2,2'-BITHIOPHENE-5-BORONIC ACID PINACOL ESTER, 97% 5-(5-hexylthiophen-2-yl)thiophene-2-boronic acid pinacol ester 2-(5′-Hexyl-2,2′-bithien-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 4,4,5,5-Tetramethyl-2-[5′-hexyl-2,2′-bithien-5-yl]-1,3,2-dioxaborolane 2-(5'-Hexyl-[2,2'-bithiophen]-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 1,3,2-Dioxaborolane, 2-(5'-hexyl[2,2'-bithiophen]-5-yl)-4,4,5,5-tetramethyl- 2-[5-(5-hexylthiophen-2-yl)thiophen-2-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 5μ-N-Hexyl-2,2μ-bithiophene-5-boronic acid pinacol ester, 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5μ-N-hexyl-2,2μ-bithiophene, 5-Hexyl-5μ-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,2μ-bithiophene | [Molecular Formula]
C20H29BO2S2 | [MDL Number]
MFCD05664380 | [MOL File]
579503-59-6.mol | [Molecular Weight]
376.38 |
Chemical Properties | Back Directory | [Melting point ]
36-40 °C(lit.) | [Boiling point ]
472.5±45.0 °C(Predicted) | [density ]
1.10±0.1 g/cm3(Predicted) | [Fp ]
110 °C | [storage temp. ]
2-8°C(protect from light) |
Hazard Information | Back Directory | [Uses]
Reagent use for
- Suzuki-Miyaura cross-coupling reactions and shape-shifting in contorted dibenzotetrathienocoronenes
- Oligothiophene self-assembly induction into fibers with tunable shape and function
- Stille coupling and p-conjugated packing structure and hole mobility of bithiophene-bithiazole copolymers with alkyl-thiophene side chains
Reagent used in Preparation of
- Solution-processed ambipolar field-effect transistor
- Light harvesting small molecules for use in solution-processed small molecule bulk heterojunction solar cell devices
- Light-emitting diode (OLED) materials
- Unsymmetric substituted benzothiadiazole-containing vinyl monomers for RAFT polymerization
- Pd-catalyzed condensations and synthesis of isoindigo-based oligothiophenes for molecuar bulk heterojunction solar cells
- Thiophene-benzothiadiazole based donor-acceptor-donor materials
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