551907-64-3 (TP4,Thiophene-4)

快速询单

结构式：

TP4MOL文件

CAS号：

551907-64-3

中文名称：

TP4

英文名称：

Thiophene-4

分子式：

C₁₆H₁₁F₅N₂O₄S

分子量：

422.326560258865

TP4(551907-64-3)名称与标识符

名称

英文别名：

Thiophene-4;5-(Aminocarbonyl)-4-methyl-2-[(pentafluorobenzoyl)amino]-3-thiophenecarboxylic acid ethyl ester;3-Thiophenecarboxylic acid, 5-(aminocarbonyl)-4-methyl-2-[(2,3,4,5,6-pentafluorobenzoyl)amino]-, ethyl ester;Thiophene-4 >=98% (HPLC);TP4;

标识符

MDL：

MFCD01353700

InChIKey：

ANCBHJKEYPZCTE-UHFFFAOYSA-N

Inchi：

1S/C16H11F5N2O4S/c1-3-27-16(26)5-4(2)12(13(22)24)28-15(5)23-14(25)6-7(17)9(19)11(21)10(20)8(6)18/h3H2,1-2H3,(H2,22,24)(H,23,25)

SMILES：

C1(NC(=O)C2=C(F)C(F)=C(F)C(F)=C2F)SC(C(N)=O)=C(C)C=1C(OCC)=O

TP4(551907-64-3)物化性质

实验特性

溶解度 : DMSO: soluble20mg/mL, clear

TP4(551907-64-3)安全信息

危险品运输编号： NONH for all modes of transport
储存条件： 2-8°C

TP4(551907-64-3)相关文献

1. DMAP mediated one-pot domino thienannulation: a versatile, regioselective and green mechanochemical route to naphtho[2,3-b]thiophenes
Gaurav Shukla,Girijesh Kumar Verma,Anugula Nagaraju,Rajiv Kumar Verma,Keshav Raghuvanshi,Maya Shankar Singh RSC Adv. 2013 3 13811
2. The effect of 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane charge transfer dopants on the conformation and aggregation of poly(3-hexylthiophene)
Jian Gao,John D. Roehling,Yongle Li,Hua Guo,Adam J. Moulé,John K. Grey J. Mater. Chem. C 2013 1 5638
3. Effects of a heteroatomic benzothienothiophenedione acceptor on the properties of a series of wide-bandgap photovoltaic polymers
Xinxin Huang,Kangkang Weng,Lijun Huo,Bingbing Fan,Chunhe Yang,Xiaobo Sun,Yanming Sun J. Mater. Chem. C 2016 4 9052
4. A D–A copolymer of dithienosilole and a new acceptor unit of naphtho[2,3-c]thiophene-4,9-dione for efficient polymer solar cells
Chaohua Cui,Xi Fan,Maojie Zhang,Jing Zhang,Jie Min,Yongfang Li Chem. Commun. 2011 47 11345
5. Regioselective α- and β-metallations of thiophene derivatives bearing the 4,4-dimethyloxazolin-2-yl group. Application of the method to syntheses of 2,3- and 2,5-disubstituted thiophene derivatives
Andrew J. Carpenter,Derek J. Chadwick J. Chem. Soc. Perkin Trans. 1 1985 173
6. A new benzo[1,2-b:4,5-b′]difuran-based copolymer for efficient polymer solar cells
Xuewen Chen,Bo Liu,Yingping Zou,Lu Xiao,Xiuping Guo,Yuehui He,Yongfang Li J. Mater. Chem. 2012 22 17724
7. Integrating theory, synthesis, spectroscopy and device efficiency to design and characterize donor materials for organic photovoltaics: a case study including 12 donors
S. D. Oosterhout,N. Kopidakis,Z. R. Owczarczyk,W. A. Braunecker,R. E. Larsen,E. L. Ratcliff,D. C. Olson J. Mater. Chem. A 2015 3 9777
8. Gas-phase heteroaromatic substitution. Part 6. Alkylation of pyrrole, N-methylpyrrole, furan, and thiophene by isopropyl cation
Giuseppe Laguzzi,Maurizio Speranza J. Chem. Soc. Perkin Trans. 2 1987 857
9. Synthesis and photovoltaic properties of D–A copolymers of benzodithiophene and naphtho[2,3-c]thiophene-4,9-dione
Chaohua Cui,Haijun Fan,Xia Guo,Maojie Zhang,Youjun He,Xiaowei Zhan,Yongfang Li Polym. Chem. 2012 3 99
10. One-step synthesis of 2,3-dihydronaphtho[2,3-b]thiophene-4,9-diones by a new regioselective [3 + 2] photoaddition of photogenerated 2-mercapto-1,4-naphthoquinone with alkenes
Hiroshi Suginome,Kazuhiro Kobayashi,Atsushi Konishi,Hiroki Minakawa,Hideo Sakurai J. Chem. Soc. Chem. Commun. 1993 807