374024
3-Methoxythiophene
98%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C5H6OS
CAS Number:
Molecular Weight:
114.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
106404
Assay:
98%
Form:
liquid
InChI
1S/C5H6OS/c1-6-5-2-3-7-4-5/h2-4H,1H3
SMILES string
COc1ccsc1
InChI key
RFSKGCVUDQRZSD-UHFFFAOYSA-N
assay
98%
form
liquid
Quality Level
bp
80-82 °C/65 mmHg (lit.)
density
1.143 g/mL at 25 °C (lit.)
Related Categories
General description
3-Methoxythiophene is a thiophene. The intramolecular and intermolecular geometries of crystals of 3-methoxythiophene were studied. Spectroscopic studies of bipolarons derived from oligomerized 3-methoxythiophene in solution has been reported. The electropolymerization of 3-methoxythiophene on Pt and Fe electrodes in an aqueous micellar medium containing sodium dodecyl sulfate and 10-3M bithiophene has been reported. Thin polymer films of 3-methoxythiophene at the cathode in a direct current discharge have been prepared.
signalword
Warning
hcodes
Hazard Classifications
Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
120.2 °F - closed cup
flash_point_c
49 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Electrosynthesis and characterization of poly (3-methoxythiophene)-polybithiophene composite films prepared in micellar media on Pt and Fe substrates.
Dieng MaM, et al.
Physical Chemistry Chemical Physics, 1(8), 1731-1734 (1999)
Paolo Bollella et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 21(1), 120-128 (2019-08-14)
Biocatalytic buckypaper electrodes modified with pyrroloquinoline quinone (PQQ)-dependent glucose dehydrogenase and bilirubin oxidase for glucose oxidation and oxygen reduction, respectively, were prepared for their use in a biofuel cell. A small (millimeter-scale; 2×3×2 mm3 ) enzyme-based biofuel cell was tested in
Martina Marinelli et al.
Chirality, 32(12), 1361-1376 (2020-11-17)
Novel optically active oligothiophenes bearing electron-donating chiral side chains have been prepared by synthetic methods suitable to achieve regioregular head-to-tail and head-to-head/tail-to-tail derivatives. In particular, the chiral (S)-(2-methyl)butyl moiety was linked at position 3 of the thiophene ring through heteroatoms
Spectroscopic studies of bipolarons from oligomerized 3-methoxythiophene in solution.
Chang A-C and Miller LL.
Synthetic Metals, 22(1), 71-78 (1987)
Blake et al.
Acta crystallographica. Section B, Structural science, 55(Pt 6), 963-974 (2000-08-06)
The intramolecular and intermolecular geometries of six thiophenes carrying oxygen-containing substituents have been determined. Crystals of 2-methoxythiophene and 3-methoxythiophene were grown in situ on a diffractometer from liquid samples. The 2-methoxy group introduces significant distortions to the thiophene nucleus and
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service