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Merck
CN

195944

2-Thiopheneacetic acid

98%

Synonym(s):

2-Thienylacetic acid

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About This Item

Empirical Formula (Hill Notation):
C6H6O2S
CAS Number:
Molecular Weight:
142.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-639-8
Beilstein/REAXYS Number:
114551
MDL number:
Assay:
98%
Form:
powder
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Quality Level

assay

98%

form

powder

bp

160 °C/22 mmHg (lit.)

mp

63-64 °C (lit.)

SMILES string

OC(=O)Cc1cccs1

InChI

1S/C6H6O2S/c7-6(8)4-5-2-1-3-9-5/h1-3H,4H2,(H,7,8)

InChI key

SMJRBWINMFUUDS-UHFFFAOYSA-N

General description

Adsorption of 2-thiopheneacetic acid on XAD-4, NDA-100 and ND-90 resin has been investigated. A new polymeric complex of Cu(II) and 2-thiopheneacetic acid has been synthesized and characterized by IR and Raman spectroscopy.

Application

2-Thiopheneacetic acid was used in the preparation of rosette-like nanoscale Au materials.


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges



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Synthesis, X-ray crystal structure and vibrational spectra of a polymeric copper (II) complex with 2-thiopheneacetic acid.
Drozdzewski P, et al.
Polyhedron, 23(10), 1785-1792 (2010)
Study of Adsorption of 2-Thiopheneacetic Acid on Three Adsorbent Resins.
Wei R, et al.
Acta Polymerica Sinica / Gao Fen Zi Xue Bao, 4, 471-477 (2004)
Hye-Seon Shin et al.
ACS applied materials & interfaces, 5(4), 1429-1435 (2013-01-23)
Rosette-like nanoscale Au materials were simply prepared through one-pot reduction of the AuCl₄⁻ precursor by 2-thiopheneacetic acid (2-TAA) without extra surface capping ligands at room temperature. 2-TAA underwent polymerization into polythiophene derivatives while the AuCl₄⁻ precursor was simultaneously reduced into



Global Trade Item Number

SKUGTIN
195944-25G04061838761866