632961
5′-Hexyl-2,2′-bithiophene-5-boronic acid pinacol ester
97%
Sinonimo/i:
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, 5′-N-Hexyl-2,2′-bithiophene-5-boronic acid pinacol ester, 5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5′-N-hexyl-2,2′-bithiophene, 5-Hexyl-5′-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,2′-bithiophene
About This Item
Prodotti consigliati
Livello qualitativo
Saggio
97%
Stato
solid
Punto di fusione
36-40 °C (lit.)
Stringa SMILE
CCCCCCc1ccc(s1)-c2ccc(s2)B3OC(C)(C)C(C)(C)O3
InChI
1S/C20H29BO2S2/c1-6-7-8-9-10-15-11-12-16(24-15)17-13-14-18(25-17)21-22-19(2,3)20(4,5)23-21/h11-14H,6-10H2,1-5H3
XTTRNSNHDCYSEL-UHFFFAOYSA-N
Categorie correlate
Applicazioni
- 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
Avvertenze
Warning
Indicazioni di pericolo
Classi di pericolo
Acute Tox. 4 Oral
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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Articoli
This brochure contains a comprehensive selection of boronic acids, boronic acid esters, diboron esters, and transition-metal catalysts useful for the Suzuki–Miyaura coupling reaction
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