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
登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式（希尔记法）:
C16H27BO2S
化学文摘社编号:
分子量:
294.26
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
MDL number:
产品名称
3-己基噻吩-2-硼酸频哪醇酯, 95%
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
SMILES string
CCCCCCc1ccsc1B2OC(C)(C)C(C)(C)O2
InChI key
XCXAUPBHQCCWCI-UHFFFAOYSA-N
assay
95%
form
liquid
refractive index
n20/D 1.490-1.499
density
0.983 g/mL at 25 °C
Quality Level
Application
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
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
>230.0 °F
flash_point_c
> 110 °C
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
法规信息
新产品
此项目有
Photophysical and Electrochemical Properties of Thiophene-Based 2-Arylpyridines
Coluccini, C.; et al.
European Journal of Organic Chemistry, 28, 5587-5598 (2011)
p/n Switching of Ambipolar Bithiazole-Benzothiadiazole-Based Polymers in Photovoltaic Cells
Balan, B.; et al.
Macromolecules, 45, 2709-2719 (2012)
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
Preparation, structure, and spectral properties of cyclophanes consisting of oligothiophene units
Tsuge, A.; et al.
Chemistry Letters (Jpn), 37, 870-871 (2008)
Tae-Hyuk Kwon et al.
The Journal of organic chemistry, 76(10), 4088-4093 (2011-04-14)
A one-pot synthesis of 2,6-dibromodithieno[3,2-b;2',3'-d]thiophene (dibromo-DTT, 4) was developed. A key step was bromodecarboxylation of DTT-2,6-dicarboxylic acid, obtained by saponification of the diester 1. The donor-acceptor dye DAHTDTT (13), based on a central 2,6-bis[2'-(3'-hexylthienyl)]dithieno[3,2-b;2',3'-d]thiophene core (9), was prepared and incorporated
商品
Oligothiophenes are important organic electronic materials which can be produced using synthetic intermediates and Suzuki coupling.
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持