| Weight | 114.169 g/mol |
|---|---|
| Formula | C5H6OS |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
3-Methoxythiophene (17573-92-1)
Score:
#3 in Electrochemistry
,
#315 in Materials science
,
#2032 in Physics
,
#6335 in Chemistry
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- Electrochemical and spectroscopic properties of poly(3-methoxythiophene) electrosynthesized in an aqueous micellar medium (Synthetic Metals, 1998)
- Characterization and spectroelectrochemical studies of soluble polymerized 3-methoxythiophene (Journal of Electroanalytical Chemistry, 1987)
- Direct CH Arylation of 3-Methoxythiophene Catalyzed by Pd. Application to a more Efficient Synthesis of -Alkoxy-oligothiophene Derivatives. (Tetrahedron Letters, 2006)
- Electrodeposition of conductive poly(3-methoxythiophene) in ionic liquid microemulsions (Journal of Electroanalytical Chemistry, 2009)
- Synthesis and photoelectric property of poly (3-methoxythiophene)/titanium dioxide complexes (Solar Energy Materials and Solar Cells, 2010)
- Spectroscopic studies of bipolarons from oligomerized 3-methoxythiophene in solution (Synthetic Metals, 1987)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=CSC=C1
-
InChIKeyRFSKGCVUDQRZSD-UHFFFAOYSA-N
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