3,4-Dimethoxythiophene

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Catalog Number
ACM51792348-2
Product Name
3,4-Dimethoxythiophene
Structure
Structure
CAS
51792-34-8
Category
Thiophenes
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.
Synonyms
Thiophene, 3,4-Dimethoxy-
IUPAC Name
3,4-dimethoxythiophene
Molecular Weight
144.19
Molecular Formula
C6H8O2S
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
Melting Point
−20°C
Flash Point
106.7 °C
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.
Storage
room temp
Assay
97%
Complexity
77.1
Covalently-Bonded Unit Count
1
Exact Mass
144.024501g/mol
Features And Benefits
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Formal Charge
0
H-Bond Acceptor
3
H-Bond Donor
0
Heavy Atom Count
9
MDL Number
MFCD01096546
Monoisotopic Mass
144.024501g/mol
NACRES
NA.23
Packaging
Packaging
5 g in glass bottle
PubChem ID
24884971
Quality Level
100
Refractive Index
n20/D 1.5409
Rotatable Bond Count
2
Storage Temperature
−20°C
XLogP3
1.5
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