Catalog Number
ACM51792348-2
Product Name
3,4-Dimethoxythiophene
Category
Other Electronic Materials; Synthetic Tools and Reagents
Synonyms
Thiophene, 3,4-Dimethoxy-
Description
3,4-Dimethoxythiophene (DMOT) is a monomer and a precursor which can be synthesized by ring closure reaction of 2,3-dimethoxy-1,3-butadiene and sulfur dichloride in hexane medium. It is an oligothiphene that is majorly used in the development of electroactive materials for organic electronics based applications.
IUPAC Name
3,4-dimethoxythiophene
Canonical SMILES
COc1cscc1OC
InChI
1S/C6H8O2S/c1-7-5-3-9-4-6(5)8-2/h3-4H,1-2H3
InChI Key
ZUDCKLVMBAXBIF-UHFFFAOYSA-N
Boiling Point
100-102 °C/10-11 mmHg
Density
1.209 g/mL at 25 °C
Appearance
Colourless Solid
Application
Building block in the synthesis of an N2S2-N4 porphyrin dyad used to study photoinduced energy transfer.
DMOT can be trans-esterified to form 3,4-ethylenendioxythiophene (EDOT). It can further be polymerized to produce PEDOT which can be used as a conductive polymer in π-conjugated systems. It can be polymerized to form poly(dimethoxythiphenes) which can potentially be used in the fabrication energy storage devices on electrochemical doping.
Covalently-Bonded Unit Count
1
Exact Mass
144.024501g/mol
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Monoisotopic Mass
144.024501g/mol
Packaging
Packaging
5 g in glass bottle
Refractive Index
n20/D 1.5409