所有图片(2)
About This Item
经验公式（希尔记法）:
C16H27BO2S
CAS号:
分子量:
294.26
MDL编号:
UNSPSC代码:
12352103
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
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
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)
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
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)
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)
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.
联系技术服务部门