3,3',5,5'-四溴-2,2'-联噻吩 | 125143-53-5
3,3',5,5'-四溴-2,2'-联噻吩
3,3',5,5'-Tetrabromo-2,2'-bithiophene
125143-53-5
C8H2S2Br4
481.84748
名称和标识符
MDL |
MFCD00114807 |
InChIKey |
MOMHMPZSZNZLAK-UHFFFAOYSA-N |
Inchi |
InChI=1S/C8H2Br4S2/c9-3-1-5(11)13-7(3)8-4(10)2-6(12)14-8/h1-2H |
SMILES |
BrC1=CC(Br)=C(S1)C1=C(Br)C=C(Br)S1 |
别名信息
- 中文别名 -
- 3,3',5,5'-四溴-2,2'-联噻吩
- 3,3 ,5,5 -四溴-2,2 -联噻吩
- 3,3',5,5'-Tetrabromo-2,2'-bithiophene 3,3',5,5'-四溴-2,2'-联噻吩
- 3,3',5,5'-四溴-
2,2'-联噻吩
- 3,3'',5,5''-四溴-2,2''-联噻吩
- 花生酸二十五烷酯
- 3,3’,5,5’-四溴-2,2’-联噻吩
- 3,3,5,5-四溴联噻吩
- 3,5-二溴-2-(3,5-二溴噻吩-2-)噻吩
- 3,3',5,5'-四溴-2,2'-联噻吩 100G
- 英文别名 -
- 3,3',5,5'-Tetrabromo-2,2'-bithiophene
- 3,5-dibromo-2-(3,5-dibromothiophen-2-yl)thiophene
- 3,3,5,5-Tetrabromo-2,2-Bithiophene
物化性质
实验特性
LogP |
6.52660 |
PSA |
56.48000 |
折射率 |
1.72 |
沸点 |
371°C at 760 mmHg |
熔点 |
138.0 to 144.0 deg-C |
闪点 |
371 °C at 760 mmHg |
密度 |
2.428 |
计算特性
精确分子量 |
477.63300 |
氢键供体数量 |
0 |
氢键受体数量 |
0 |
可旋转化学键数量 |
1 |
同位素质量 |
477.633 |
重原子数量 |
14 |
复杂度 |
194 |
同位素原子数量 |
0 |
确定原子立构中心数量 |
0 |
不确定原子立构中心数量 |
0 |
确定化学键立构中心数量 |
0 |
不确定化学键立构中心数量 |
0 |
共价键单元数量 |
1 |
疏水参数计算参考值(XlogP) |
6.4 |
互变异构体数量 |
无 |
表面电荷 |
0 |
拓扑分子极性表面积 |
56.5A^2 |
海关数据
海关编码 |
2934999090 |
海关数据 |
中国海关编码:
2934999090
概述:
2934999090. 其他杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%
申报要素:
品名, 成分含量, 用途
Summary:
2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
|
相关文献
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1.
A versatile and efficient synthesis of bithiophene-based dicarboxaldehydes from a common synthon
Achala Bhuwalka,Jared F. Mike,Jeremy J. Intemann,Arkady Ellern,Malika Jeffries-EL Org. Biomol. Chem. 2015 13 9462
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Electropolymerizable 3Dπ-conjugated architectures with ethylenedioxythiophene (EDOT) end-groups as precursors of electroactive conjugated networks
Flavia Piron,Philippe Leriche,Ion Grosu,Jean Roncali J. Mater. Chem. 2010 20 10260
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Bhooshan C. Popere,Andrea M. Della Pelle,Ambata Poe,Ganapathy Balaji,S. Thayumanavan Chem. Sci. 2012 3 3093
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Iridium(iii) complexes with the dithieno[3,2-b:2′,3′-d]phosphole oxide group and their high optical power limiting performances
Zhao Liu,Yanmin Xu,Ling Yue,Ming Li,Xiaolong Yang,Yuanhui Sun,Lihe Yan,Guijiang Zhou Dalton Trans. 2020 49 4967
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Iodine capture in porous organic polymers and metal–organic frameworks materials
Wei Xie,Di Cui,Shu-Ran Zhang,Yan-Hong Xu,Dong-Lin Jiang Mater. Horiz. 2019 6 1571
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A series of thiophene- and nitrogen-rich conjugated microporous polymers for efficient iodine and carbon dioxide capture
Li Wang,Chan Yao,Wei Xie,Guangjuan Xu,Shuran Zhang,Yanhong Xu New J. Chem. 2021 45 19636
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8.
Porous sorbents for the capture of radioactive iodine compounds: a review
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The role of borole in a fully conjugated electron-rich system
Sanghoon Kim,Kee-hyung Song,Sang Ook Kang,Jaejung Ko Chem. Commun. 2004 68
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10.
Influence of the N-heterocycle substituent of the dithieno[3,2-b:2′,3′-d]pyrrole (DTP) spacer as well as sensitizer adsorption time on the photovoltaic properties of arylamine organic dyes
Zhihui Wang,Mao Liang,Yujie Hao,Yue Zhang,Lina Wang,Zhe Sun,Song Xue J. Mater. Chem. A 2013 1 11809
参考资料
Reaxys RN |
212497 |
Beilstein |
19(4)266 |
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「3,3',5,5'-四溴-2,2'-联噻吩」125143-53-5
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