3,4-Ethylenedioxythiophene
Catalog Number
ACM126213501-2
CAS
126213-50-1
IUPAC Name
2,3-Dihydrothieno[3,4-b][1,4]dioxine
Synonyms
EDOT
Application
EDOT can be polymerized to form poly(3,4-ethylenedioxythiophene) (PEDOT) for use as an electrochromic polymer (EC) based coating for a variety of s like solid state organic electrochemical supercapacitors (OESCs), electrochromic devices (ECDs), and carbon nanotubes (CNTs) based electrochemical devices for diabetes monitoring.
It can be used:
As a reductant in a one-pot synthesis of gold nanoparticles from HAuCl4 (254169).
As a starting material used in palladium-catalyzed mono- and bis-arylation reactions.
In the synthesis of conjugated polymers and copolymers, with potential optical s.
It can be used:
As a reductant in a one-pot synthesis of gold nanoparticles from HAuCl4 (254169).
As a starting material used in palladium-catalyzed mono- and bis-arylation reactions.
In the synthesis of conjugated polymers and copolymers, with potential optical s.
Molecular Weight
142.18
Molecular Formula
C6H6O2S
Product Information
Description
3,4-Ethylenedioxythiophene (EDOT) is an electro-active conductive monomer with a thiol group that combines an electron donor and electron acceptor in a donor-acceptor-donor arrangement.
Monomer used in the synthesis of conducting polymers.
Monomer used in the synthesis of conducting polymers.
Canonical SMILES
C1COC2=CSC=C2O1
InChI
InChI=1S/C6H6O2S/c1-2-8-6-4-9-3-5(6)7-1/h3-4H,1-2H2
InChI Key
GKWLILHTTGWKLQ-UHFFFAOYSA-N
Boiling Point
210.5±19.0 °C/760mmHg (lit.)
Melting Point
10 °C
Flash Point
81.1±21.5 °C
Purity
95%+
Density
1.3±0.1 g/cm³
Solubility
Slightly soluble in water
Appearance
Liquid
Storage
2-8 °C
Complexity
95.2
Covalently-Bonded Unit Count
1
Exact Mass
142.0088506
Heavy Atom Count
9
MDL Number
MFCD02093622
Monoisotopic Mass
142.0088506
Refractive Index
n20/D 1.571 (lit.)
Rotatable Bond Count
0
Topological Polar Surface Area
46.7 Ų
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