3,4-Propylenedioxythiophene - CAS 155861-77-1
Catalog: |
BB011169 |
Product Name: |
3,4-Propylenedioxythiophene |
CAS: |
155861-77-1 |
Synonyms: |
3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine |
Application: |
PRODOT can be used as a conjugated polymer in the fabrication of dye sensitized solar cells (DSSCs), sensors and electrochromic materials. |
IUPAC Name: | 3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine |
Description: | PRODOT can be used as a conjugated polymer in the fabrication of dye sensitized solar cells (DSSCs), sensors and electrochromic materials. |
Molecular Weight: | 156.20 |
Molecular Formula: | C7H8O2S |
Canonical SMILES: | C1COC2=CSC=C2OC1 |
InChI: | InChI=1S/C7H8O2S/c1-2-8-6-4-10-5-7(6)9-3-1/h4-5H,1-3H2 |
InChI Key: | WNOOCRQGKGWSJE-UHFFFAOYSA-N |
Boiling Point: | 229.704 °C at 760 mmHg |
Purity: | 97 % |
Density: | 1.244 g/cm3 |
MDL: | MFCD08276807 |
LogP: | 1.90940 |
Publication Number | Title | Priority Date |
CN-113336922-A | Electrochromic polymer with high transmittance from neutral cyan to oxidized | 20210621 |
CN-113354798-A | Thiophene-3, 4-ethylenedioxythiophene derivative polymer and preparation method and application thereof | 20210621 |
JP-2021093377-A | Method for manufacturing conductive particles | 20210304 |
KR-102217021-B1 | Solder composition comprisng conductive polymer and method of combination conductive pattern using the same | 20210104 |
KR-20210005746-A | Solder composition comprisng conductive polymer and method of combination conductive pattern using the same | 20210104 |
PMID | Publication Date | Title | Journal |
22744748 | 20120814 | A new generation of platinum and iodine free efficient dye-sensitized solar cells | Physical chemistry chemical physics : PCCP |
22136160 | 20120101 | Composite electronic materials based on poly(3,4-propylenedioxythiophene) and highly charged poly(aryleneethynylene)-wrapped carbon nanotubes for supercapacitors | ACS applied materials & interfaces |
21678981 | 20110727 | Structural, optical, and electronic properties of a series of 3,4-propylenedioxythiophene oligomers in neutral and various oxidation States | Journal of the American Chemical Society |
21395243 | 20110401 | Material strategies for black-to-transmissive window-type polymer electrochromic devices | ACS applied materials & interfaces |
20931950 | 20101104 | Mechanistic aspects of radiation-induced oligomerization of 3,4-ethylenedioxythiophene in ionic liquids | The journal of physical chemistry. A |
Complexity: | 106 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 156.02450067 |
Formal Charge: | 0 |
Heavy Atom Count: | 10 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 156.02450067 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 46.7 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 1.7 |
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