632961
5′-Hexyl-2,2′-bithiophene-5-boronic acid pinacol ester
97%
Sinônimo(s):
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
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About This Item
Produtos recomendados
Nível de qualidade
Ensaio
97%
Formulário
solid
pf
36-40 °C (lit.)
cadeia de caracteres SMILES
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
chave InChI
XTTRNSNHDCYSEL-UHFFFAOYSA-N
Categorias relacionadas
Aplicação
- Suzuki-Miyaura cross-coupling reactions and shape-shifting in contorted dibenzotetrathienocoronenes[1]
- Oligothiophene self-assembly induction into fibers with tunable shape and function[2]
- Stille coupling and p-conjugated packing structure and hole mobility of bithiophene-bithiazole copolymers with alkyl-thiophene side chains[3]
Reagent used in Preparation of
- Solution-processed ambipolar field-effect transistor[4]
- Light harvesting small molecules for use in solution-processed small molecule bulk heterojunction solar cell devices[5]
- Light-emitting diode (OLED) materials[6]
- Unsymmetric substituted benzothiadiazole-containing vinyl monomers for RAFT polymerization[7]
- Pd-catalyzed condensations and synthesis of isoindigo-based oligothiophenes for molecuar bulk heterojunction solar cells[8]
- Thiophene-benzothiadiazole based donor-acceptor-donor materials[9]
Palavra indicadora
Warning
Frases de perigo
Classificações de perigo
Acute Tox. 4 Oral
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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Artigos
Oligothiophenes are important organic electronic materials which can be produced using synthetic intermediates and Suzuki coupling.
Suzuki-Miyaura cross-coupling reaction is extensively used in organic chemistry, polymer science, and pharmaceutical industries.
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