697400
3-己基噻吩-2-硼酸频哪醇酯
95%
别名:
2-(3-己基-2-噻吩基)-4,4,5,5-四甲基-1,3,2-二氧杂硼烷
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关于此项目
经验公式（希尔记法）:
C16H27BO2S
CAS Number:
分子量:
294.26
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22
质量水平
方案
95%
表单
liquid
折射率
n20/D 1.490-1.499
密度
0.983 g/mL at 25 °C
SMILES字符串
CCCCCCc1ccsc1B2OC(C)(C)C(C)(C)O2
InChI
1S/C16H27BO2S/c1-6-7-8-9-10-13-11-12-20-14(13)17-18-15(2,3)16(4,5)19-17/h11-12H,6-10H2,1-5H3
InChI key
XCXAUPBHQCCWCI-UHFFFAOYSA-N
应用
Reagent used for
Reagent used in Preparation of
- Suzuki-Miyaura cross-coupling reactions
- p-type/n-type switching of ambipolar bithiazole-benzothiadiazole-based polymers in solar cells
- Hierarchical self-assembly of semiconductor functionalized peptide a-helixes and optoelectronic properties
Reagent used in Preparation of
- Photovoltaic materials, polymers, and thiophene-based compounds with photophysical, electrochemical, and fluorescent properties
- Polymer solar cells for Low band gap poly(1,4-arylene-2,5-thienylene)s with benzothiadiazole units
- Dithienothiophene-based dyes for dye-sensitized solar cells
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
>230.0 °F
闪点(°C)
> 110 °C
个人防护装备
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
法规信息
新产品
p/n Switching of Ambipolar Bithiazole-Benzothiadiazole-Based Polymers in Photovoltaic Cells
Balan, B.; et al.
Macromolecules, 45, 2709-2719 (2012)
Photophysical and Electrochemical Properties of Thiophene-Based 2-Arylpyridines
Coluccini, C.; et al.
European Journal of Organic Chemistry, 28, 5587-5598 (2011)
Rohan J Kumar et al.
Journal of the American Chemical Society, 133(22), 8564-8573 (2011-05-17)
To determine the ability of semiconductors templated by α-helical polypeptides to form higher order structures and the charge carrier properties of the supramolecular assemblies, L-lysine was functionalized with a sexithiophene organic semiconductor unit via iterative Suzuki coupling and the click
Photovoltaic response to structural modifications on a series of conjugated polymers based on 2-aryl-2H-benzotriazoles
Pasker, F. M.; et al.
Journal of Polymer Science Part A: Polymer Chemistry, 49, 5001-5011 (2011)
Low band gap poly(1,4-arylene-2,5-thienylene)s with benzothiadiazole units: Synthesis, characterization and application in polymer solar cells
Operamolla, A.; et al.
Solar Energy Mat. and Solar Cells, 95, 3490-3503 (2011)
商品
Oligothiophenes are important organic electronic materials which can be produced using synthetic intermediates and Suzuki coupling.
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