5′-Hexyl-2,2′-bithiophene-5-boronic acid pinacol ester

• Catalog No.: 632961
• CAS Number: 579503-59-6
• M. F.: C20H29BO2S2
• M. W.: 376.38406
• Purity: 97%

SYNONYMS

• Title: 5′-己基-2,2′-联噻吩-5-硼酸频哪醇酯
• IUPAC name: 2-[5-(5-hexylthiophen-2-yl)thiophen-2-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• IUPAC Traditional name: 2-[5-(5-hexylthiophen-2-yl)thiophen-2-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• Synonyms: 5′-N-己基-2,2′-联噻吩-5-硼酸频哪醇酯; 5-(4,4,5,5-四甲基-1,3,2-二氧杂硼烷-2-基)-5′-N-己基-2,2′-联噻吩; 5-己基-5′-(4,4,5,5-四甲基-1,3,2-二氧杂硼烷-2-基)-2,2′-联噻吩; 5-Hexyl-5′-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,2′-bithiophene; 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

DATABASE IDS

• MDL Number: MFCD05664380
• CAS Number: 579503-59-6
• PubChem SID: 24882530

PROPERTIES

• Empirical Formula (Hill Notation): C20H29BO2S2
• Purity: 97%
• Melting Point: 36-40 °C(lit.)
• GHS Signal Word: Warning
• GHS Hazard statements: H302
• European Hazard Symbols: Harmful (Xn)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• Risk Statements: 22
• Safety Statements: 36
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1, 5 g in glass bottle
Application
Reagent use for
• Suzuki-Miyaura cross-coupling reactions and shape-shifting in contorted dibenzotetrathienocoronenes1
• Oligothiophene self-assembly induction into fibers with tunable shape and function2
• Stille coupling and p-conjugated packing structure and hole mobility of bithiophene-bithiazole copolymers with alkyl-thiophene side chains3 Reagent used in Preparation of
• Solution-processed ambipolar field-effect transistor4
• Light harvesting small molecules for use in solution-processed small molecule bulk heterojunction solar cell devices5
• Light-emitting diode (OLED) materials6
• Unsymmetric substituted benzothiadiazole-containing vinyl monomers for RAFT polymerization7
• Pd-catalyzed condensations and synthesis of isoindigo-based oligothiophenes for molecuar bulk heterojunction solar cells8
• Thiophene-benzothiadiazole based donor-acceptor-donor materials9

Description (简体中文)

包装
1, 5 g in glass bottle
Application
Reagent use for
• Suzuki-Miyaura cross-coupling reactions and shape-shifting in contorted dibenzotetrathienocoronenes1
• Oligothiophene self-assembly induction into fibers with tunable shape and function2
• Stille coupling and p-conjugated packing structure and hole mobility of bithiophene-bithiazole copolymers with alkyl-thiophene side chains3 Reagent used in Preparation of
• Solution-processed ambipolar field-effect transistor4
• Light harvesting small molecules for use in solution-processed small molecule bulk heterojunction solar cell devices5
• Light-emitting diode (OLED) materials6
• Unsymmetric substituted benzothiadiazole-containing vinyl monomers for RAFT polymerization7
• Pd-catalyzed condensations and synthesis of isoindigo-based oligothiophenes for molecuar bulk heterojunction solar cells8
• Thiophene-benzothiadiazole based donor-acceptor-donor materials9