Substance
ID:326635
Names and Identifiers
IUPAC name
2H,3H-thieno[3,4-b][1,4]dioxine
Synonyms
EDOT2,3-Dihydrothieno[3,4-b]-1,4-dioxin3,4-Ethylenedioxythiophene2,3-二氢噻吩并[3,4-b]-1,4-二氧六环3,4-乙烯二氧噻吩
IUPAC Traditional name
2H,3H-thieno[3,4-b][1,4]dioxine
Properties
Safety Information
European Hazard Symbols
Harmful (Xn)Personal Protective Equipment
Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements
P280-P305+P351+P338-P312
Safety Statements
26-36
Packing Group
3
German water hazard class
2
GHS Hazard statements
H302-H311-H319
MSDS Link
RID/ADR
UN 2810 6.1/PG 3
Hazard Class
6.1
GHS Signal Word
Danger
Storage Temperature
2-8°C
UN Number
2810
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), categories 1,2,3
Risk Statements
21/22-36
Product Information
Purity
97%
Empirical Formula (Hill Notation)
C6H6O2S
Physical Property
Density
1.331 g/mL at 25 °C(lit.)
Flash Point
104 °C
219.2 °F
Refractive Index
n20/D 1.5765(lit.)
Boiling Point
193 °C(lit.)
Molecule Details
Application
Employed as a reductant in a one-pot synthesis of gold nanoparticles from HAuCl4 (254169).1 Starting material used in palladium-catalyzed mono- and bis-arylation reactions.2
Employed in the synthesis of conjugated polymers and copolymers, with potential optical applications.
General description
Monomer used in the synthesis of conducting polymers.3,4
Packaging
10 g in glass bottle
Employed as a reductant in a one-pot synthesis of gold nanoparticles from HAuCl4 (254169).1 Starting material used in palladium-catalyzed mono- and bis-arylation reactions.2
Employed in the synthesis of conjugated polymers and copolymers, with potential optical applications.
General description
Monomer used in the synthesis of conducting polymers.3,4
Packaging
10 g in glass bottle
Molecular Spectra
No Data Available
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References
No Data Available
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