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3,4-Dimethoxythiophene, 98%
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3,4-Dimethoxythiophene, 98%
3,4-Dimethoxythiophene, 98%
3,4-Dimethoxythiophene, 98%
Thermo Scientific Chemicals

3,4-Dimethoxythiophene, 98%

CAS: 51792-34-8 | C6H8O2S | 144.188 g/mol
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Catalog number H56674.03
also known as H56674-03
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Chemical Identifiers
CAS51792-34-8
IUPAC Name3,4-dimethoxythiophene
Molecular FormulaC6H8O2S
InChI KeyZUDCKLVMBAXBIF-UHFFFAOYSA-N
SMILESCOC1=CSC=C1OC
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SpecificationsSpecification SheetSpecification Sheet
Assay (GC)98%
3,4-Dimethoxythiophene is used as an electronic materials intermediate. It is used as a starting material in the synthesis of porphyrin dyad which is used to study photoinduced energy transfer.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
3,4-Dimethoxythiophene is used as an electronic materials intermediate. It is used as a starting material in the synthesis of porphyrin dyad which is used to study photoinduced energy transfer.

Solubility
Miscible with organic solvents. Slightly miscible with water.

Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Shibasaki, K.; Watanab, M.; Kijima, M. Synthesis and characterization of soluble poly(3,4-phenylenedioxythiophene). Synth. Met. 2015,205 18-22.
  2. DiCarmine, P. M.; Schon, T. B.; McCormick, T. M.; Klein, P. P.; Seferos, D. S. Donor-Acceptor Polymers for Electrochemical Supercapacitors: Synthesis, Testing, and Theory. J. Phys. Chem. C 2014, 118 (16), 8295-8307.
  3. Kumar, P.; Kashid, V. S.; Mague, J. T.; Balakrishna, M. S. An efficient approach for the synthesis of functionalized selenoethers and selenacalix[4]thiophenes, {2,5-(μ-Se)(3,4-dialkoxythiophene)}4 Tetrahedron Lett. 2014, 55 (38), 5232-5235.