3-己基噻吩 | 1693-86-3
3-己基噻吩
3-Hexylthiophene
1693-86-3
C10H16S
168.299041748047
如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击:3-己基噻吩结构式
名称和标识符
MDL |
MFCD00143181 |
InChIKey |
JEDHEMYZURJGRQ-UHFFFAOYSA-N |
Inchi |
1S/C10H16S/c1-2-3-4-5-6-10-7-8-11-9-10/h7-9H,2-6H2,1H3 |
SMILES |
CCCCCCC1=CSC=C1 |
别名信息
- 中文别名 -
- 3-己基噻吩
- 2,5-二溴-3-癸基噻吩
- 3-正己基噻吩
- 3-己基噻吩(定做10-15天)
- 3-己基噻吩(C10H16S)
- 3-Hexylthiophene 3-己基噻吩
- 3-己基噻吩,3-Hexylthiophene
- 3-已基噻吩
- 3-己基噻吩 5G
- 3-己基噻吩,98%
- 4 3-己基噻吩98%
- 3-N-己基噻吩, 99+%
- 英文别名 -
- 3-Hexylthiophene
- 3-N-HEXYLTHIOPHENE
- HEXYLTHIOPHENE(3-)
- 4-Hexylthiophene
- 3-Hexylthiopene
- 3-Hexylthiophen
- 1-(Thien-3-yl)hexane
- 3-(Hex-1-yl)thiophene
- 3-HEXYLTHIOPHENE,98%
- 3-Hexylthiophene, 97+%
- 3-HEXYLTHIOPHENE
物化性质
实验特性
LogP |
3.87090 |
PSA |
28.24000 |
折射率 |
n20/D 1.496(lit.) |
水溶性 |
Partly soluble in water. |
沸点 |
103°C/10mmHg(lit.) |
熔点 |
-39.15°C (estimate) |
蒸气压 |
0.1±0.4 mmHg at 25°C |
闪点 |
华氏:98.6 °F 摄氏:37 °C
|
颜色与性状 |
未确定。 |
溶解性 |
未确定 |
敏感性 |
对光敏感 |
密度 |
0.936 g/mL at 25 °C(lit.) |
计算特性
精确分子量 |
168.09700 |
氢键供体数量 |
0 |
氢键受体数量 |
0 |
可旋转化学键数量 |
5 |
同位素质量 |
168.097271 |
重原子数量 |
11 |
复杂度 |
90.9 |
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) |
无 |
互变异构体数量 |
无 |
表面电荷 |
0 |
拓扑分子极性表面积 |
28.2 |
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.
Metallopolymers from direct polymerization of functionalized cobalt chalcogenide clusters and thiophene comonomers
D. A. Corbin,D. M. Shircliff,B. J. Reeves,B. M. Boardman Polym. Chem. 2017 8 3801
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2.
Synthesis and characterization of polythiophenes with alkenyl substituents
Nadia Hundt,Kumaranand Palaniappan,Prakash Sista,John W. Murphy,Jing Hao,Hien Nguyen,Eugene Stein,Michael C. Biewer,Bruce E. Gnade,Mihaela C. Stefan Polym. Chem. 2010 1 1624
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3.
Recent developments in the synthesis of regioregular thiophene-based conjugated polymers for electronic and optoelectronic applications using nickel and palladium-based catalytic systems
Bibi Amna,Humaira Masood Siddiqi,Abbas Hassan,Turan Ozturk RSC Adv. 2020 10 4322
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4.
Polymers for electronics and spintronics
Piotr Bujak,Irena Kulszewicz-Bajer,Malgorzata Zagorska,Vincent Maurel,Ireneusz Wielgus,Adam Pron Chem. Soc. Rev. 2013 42 8895
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5.
Poly(3-hexylthiophene): synthetic methodologies and properties in bulk heterojunction solar cells
Assunta Marrocchi,Daniela Lanari,Antonio Facchetti,Luigi Vaccaro Energy Environ. Sci. 2012 5 8457
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6.
Synthesis, characterization, and solution structure of all-conjugated polyelectrolyte diblock copoly(3-hexylthiophene)s
Hao Xia,Zhi Ye,Xiaofeng Liu,Juan Peng,Feng Qiu RSC Adv. 2014 4 19646
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7.
Simple procedure for mono- and bis-end-functionalization of regioregular poly(3-hexylthiophene)s using chalcogens
Ken Okamoto,Christine K. Luscombe Chem. Commun. 2014 50 5310
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8.
Role of the transition metal in Grignard metathesis polymerization (GRIM) of 3-hexylthiophene
Mahesh P. Bhatt,Harsha D. Magurudeniya,Prakash Sista,Elena E. Sheina,Malika Jeffries-EL,Benjamin G. Janesko,Richard D. McCullough,Mihaela C. Stefan J. Mater. Chem. A 2013 1 12841
-
9.
New strategy for synthesis of hydroxyl-terminated poly(3-hexylthiophene) and its block copolymer using an η3-π-allyl hydroxyl-functionalized Ni(i) initiator
Xin Min,Changchao Zhan,Ping Yan,Zhigang Ye RSC Adv. 2020 10 39814
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10.
Exciton diffusion controlled quantum efficiency in hybrid dye sensitized solar cells
Zaicheng Sun,Yajun Cheng,Maria Lechmann,Jiaoli Li,Jixue Li,Jishan Wu,Andrew Grimsdale,Klaus Müllen,Hans-Jürgen Butt,Jochen S. Gutmann Phys. Chem. Chem. Phys. 2009 11 1604
参考资料
Reaxys RN |
1617129 |
Beilstein |
1617129 |
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