3,4-Dimethoxythiophene

3,4-Dimethoxythiophene Basic information
Product Name:3,4-Dimethoxythiophene
Synonyms:3,4-DIMETHOXYTHIOPHENE 98%;3,4-dimethoxytiophene;,4-diMethoxythiophene;3,4-diMethoxy thiophene (DMOT);3,4- twoMethoxythiophene;DMOT;3,4-DIMETHOXYTHIOPHENE;AKOS BBS-00006359
CAS:51792-34-8
MF:C6H8O2S
MW:144.19
EINECS:628-711-7
Product Categories:OLED;Organic Electronics and Photonics;Thiophenes;Synthetic Tools and Reagents;Thiophene Monomers and Building Blocks;Thiophene Series
Mol File:51792-34-8.mol
3,4-Dimethoxythiophene Structure
3,4-Dimethoxythiophene Chemical Properties
Boiling point 100-102 °C/10-11 mmHg
density 1.209 g/mL at 25 °C
refractive index 1.5409
Fp 224 ºF
storage temp. -20°C
form powder to lump to clear liquid
color White or Colorless to Yellow
Water Solubility Miscible with organic solvents. Slightly miscible with water.
CAS DataBase Reference51792-34-8(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-22
Safety Statements 26-36/37/39-24/25
WGK Germany 3
HS Code 29309090
MSDS Information
3,4-Dimethoxythiophene Usage And Synthesis
Chemical PropertiesColorless to yellow to orange liquid
Uses3,4-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.
UsesBuilding block in the synthesis of an N2S2-N4 porphyrin dyad used to study photoinduced energy transfer.
Synthesis Reference(s)Journal of the American Chemical Society, 73, p. 2956, 1951 DOI: 10.1021/ja01150a525
General Description3,4-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.
5,7-Dibromo-2,3-dihydrothieno[3,4-b][1,4]dioxine 2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXIN-5-YLMETHANOL Diphenyldimethoxysilane 1-Pyrrolidineethanol, alpha-(((4-methoxy-3-thienyl)oxy)methyl)-2,2,5,5 -tetramethyl-, hydrochloride Dimethyldimethoxysilane N-(2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXIN-5-YLMETHYL)-N-METHYLAMINE 2,2',3,3'-TETRAHYDRO-[5,5'-BITHIENO[3,4-B]-1,4-DIOXIN]-7,7'-DICARBOXALDEHYDE 5-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE Dimethoxybenzene 2,3-DIHYDRO-5-(2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXIN-5-YL)THIENO[3,4-B][1,4]DIOXINE 2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE-5-CARBOXYLIC ACID 2,5-Dicarboxylic acid-3,4-ethylenedioxythiophene 1,1-Dimethoxyethane 2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE-5-CARBONITRILE 3,4-Dimethoxythiophene Thieno[3,4-b]-1,4-dioxin-5,7-dicarboxylic acid, 2,3-dihydro-, diethyl ester Tetrahydrothiophene Cephalothin sodium

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