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632961

5′-己基-2,2′-联噻吩-5-硼酸频哪醇酯

Name: 5′-己基-2,2′-联噻吩-5-硼酸频哪醇酯
Brand: ALDRICH

97%

别名:

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′-N-己基-2,2′-联噻吩-5-硼酸频哪醇酯

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About This Item

经验公式（希尔记法）:

C₂₀H₂₉BO₂S₂

CAS号:

579503-59-6

分子量:

376.38

MDL编号:

MFCD05664380

UNSPSC代码:

12352103

PubChem化学物质编号:

24882530

NACRES:

NA.22

质量水平

100

检测方案

97%

形式

solid

mp

36-40 °C (lit.)

SMILES字符串

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

InChI key

XTTRNSNHDCYSEL-UHFFFAOYSA-N

应用

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

象形图

GHS07

警示用语：

Warning

危险声明

H302

危险分类

Acute Tox. 4 Oral

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

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Benzothiadiazole-Containing Pendant Polymers Prepared by RAFT and Their Electro-Optical Properties

Haussler, M.; et al.

Macromolecules, 43, 7101-7110 (2010)

Bithiophene-bithiazole alternating copolymers with thiophene side chains: Synthesis by organometallic polycondensation and chemical properties of the copolymers

Yamamoto, T.; et al.

Journal of Polymer Science Part A: Polymer Chemistry, 49, 1508-1512 (2011)

A successful chemical strategy to induce oligothiophene self-assembly into fibers with tunable shape and function.

Francesca Di Maria et al.

Journal of the American Chemical Society, 133(22), 8654-8661 (2011-04-30)

Functional supramolecular architectures for bottom-up organic nano- and microtechnology are a high priority research topic. We discovered a new recognition algorithm, resulting from the combination of thioalkyl substituents and head-to-head regiochemistry of substitution, to induce the spontaneous self-assembly of sulfur

A modular molecular framework for utility in small-molecule solution-processed organic photovoltaic devices

Welch, G. C.; et al.

Journal of Materials Chemistry, 21, 12700-12709 (2011)

Solution-Processed Ambipolar Field-Effect Transistor Based on Diketopyrrolopyrrole Functionalized with Benzothiadiazole

Zhang, Y.; et al.

Advances in Functional Materials, 22, 97-105 (2012)

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