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About This Item
Empirical Formula (Hill Notation):
C8H10O2S
CAS Number:
Molecular Weight:
170.23
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
98%
form
liquid
refractive index
n20/D 1.509 (lit.)
bp
97-98 °C/8 mmHg (lit.)
density
1.137 g/mL at 25 °C (lit.)
functional group
ester
SMILES string
CCOC(=O)Cc1ccsc1
InChI
1S/C8H10O2S/c1-2-10-8(9)5-7-3-4-11-6-7/h3-4,6H,2,5H2,1H3
InChI key
FZBNQIWPYCUPAP-UHFFFAOYSA-N
General description
Ethyl 3-thiopheneacetate undergoes copolymerization with 3-alkylthiophene to yield poly(3-alkyl-2,5-thienylene-co-3-methyiene-ethylcarboxylate-2,5-thienylene).
Application
Ethyl 3-thiopheneacetate has been used in preparation of:
- solution-processible hybrid polymers, consisting of a polythiophene main chain and randomly distributed alkyl and oligoaniline side groups
- poly(thiophene-3-acetic acid)
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
217.4 °F - closed cup
Flash Point(C)
103.00 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Random and regioregular thiophene-based copolymers containing oligoaniline side chains: Synthesis, spectroscopic and spectroelectrochemical investigations.
Buga K, et al.
Synthetic Metals, 153(1-3), 137-140 (2005)
Postpolymerization grafting of aniline tetramer on polythiophene chain: Structural organization of the product and its electrochemical and spectroelectrochemical properties.
Buga K, et al.
Chemistry of Materials, 17(23), 5754-5762 (2005)
Construction of organic-inorganic hybrid ultrathin films self-assembled from poly (thiophene-3-acetic acid) and TiO2.
Ding H, et al.
Journal of Materials Chemistry, 12(12), 3585-3590 (2002)
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