5'-Hexyl-2,2'-bithiophene-5-boronic acid pinacol ester
Catalog Number
ACM579503596-1
Synonyms
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
IUPAC Name | 2-[5-(5-hexylthiophen-2-yl)thiophen-2-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane |
Molecular Weight | 376.38 |
Molecular Formula | C20H29BO2S2 |
Canonical 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,XTTRNSNHDCYSEL-UHFFFAOYSA-N |
InChI Key | XTTRNSNHDCYSEL-UHFFFAOYSA-N |
Melting Point | 36-40 °C (lit.) |
Application | 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 |
Storage | room temp |
Assay | 0.97 |
MDL Number | MFCD05664380 |
Packaging | 1, 5 g in glass bottle |
Quality Level | 100 |