Catalog Number
ACM579503596-1
Product Name
5'-Hexyl-2,2'-bithiophene-5-boronic acid pinacol ester
Category
Salt; Synthetic Tools and Reagents
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 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
Covalently-Bonded Unit Count
1
Exact Mass
376.170203g/mol
Monoisotopic Mass
376.170203g/mol
Packaging
1, 5 g in glass bottle