![]() 2-Thiopheneethylamine structure
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Common Name | 2-Thiopheneethylamine | ||
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CAS Number | 30433-91-1 | Molecular Weight | 127.207 | |
Density | 1.1±0.1 g/cm3 | Boiling Point | 199.7±15.0 °C at 760 mmHg | |
Molecular Formula | C6H9NS | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 74.6±20.4 °C | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Understanding the effect of surface chemistry on charge generation and transport in poly (3-hexylthiophene)/CdSe hybrid solar cells.
ACS Appl. Mater. Interfaces 3(2) , 287-92, (2011) For hybrid solar cells, interfacial chemistry is one of the most critical factors for good device performance. We have demonstrated that the size of the surface ligands and the dispersion of nanoparticles in the solvent and in the polymer are important criter... |
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The incorporation of mono- and bi-functionalized multiwall carbon nanotubes in organic photovoltaic cells.
Nanotechnology 22(26) , 265607, (2011) We have successfully prepared mono- and bi-functionalized multiwall carbon nanotubes (MWCNT) with thiophene, amine and thiophene-amine groups. The dispersion of nanotubes has been enhanced and stable optimized dispersions in organic solvents were obtained. Th... |
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Solution-phase, parallel synthesis and pharmacological evaluation of acylguanidine derivatives as potential sodium channel blockers.
Bioorg. Med. Chem. Lett. 11(24) , 3151-5, (2001) Solution-phase synthesis of various acylguanidine derivatives and the evaluation of a small library of compounds as potential sodium channel blockers are described. |
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Synthesis, anti-inflammatory and analgesic activity evaluation of some pyrimidine derivatives. Sondhi SM, et al.
Indian J. Chem. B 48(2) , 273, (2009)
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Efficient synthesis of piperazine-2,6-dione and 4-(1H-indole-2-carbonyl) piperazine-2,6-dione derivatives and their evaluation for anticancer activity. Kumar S, et al.
Med. Chem. Res. 22(10) , 4600-4609, (2013)
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