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196320

Sigma-Aldrich

3-Acetylthiophene

98%

Synonym(s):

Methyl-3-thienyl ketone

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About This Item

Empirical Formula (Hill Notation):
C6H6OS
CAS Number:
1468-83-3
Molecular Weight:
126.18
Beilstein/REAXYS Number:
107241
EC Number:
215-996-4
MDL number:
MFCD00005468
UNSPSC Code:
12352100
PubChem Substance ID:
24851752
NACRES:
NA.22

Quality Level

200

assay

98%

form

solid

bp

208-210 °C/748 mmHg (lit.)

mp

57-62 °C (lit.)

SMILES string

CC(=O)c1ccsc1

InChI

1S/C6H6OS/c1-5(7)6-2-3-8-4-6/h2-4H,1H3

InChI key

RNIDWJDZNNVFDY-UHFFFAOYSA-N

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General description

3-Acetylthiophene modified glassy carbon electrode has been used in voltammetric determination of uric acid in urine samples.

Application

3-Acetylthiophene was used in the preparation of 1-(methylthiophenylidine)-8-naphthylamine(Schiff′s base) and 1-(thiophen-3-yl)ethanone.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Sigma-Aldrich

T40606

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Electro-oxidative polymerization of Schiff-base of 1, 8-diaminonaphthaline and 3-acetylthiophene. I. Preparation and study the redox behaviour of the resulting polymer.
Hathoot AA.
Eur. Polymer J., 36(5), 1063-1071 (2000)
Ewa Rozycka-Sokolowska et al.
Acta crystallographica. Section C, Crystal structure communications, 67(Pt 6), o209-o211 (2011-06-03)
The structure of the title compound, C(6)H(6)OS, exhibits a flip-type disorder of the thiophene ring [occupancy ratio = 0.848 (3):0.152 (3)], which is typical for many thiophene derivatives. The puckered thiophene ring is essentially coplanar with the plane formed by
Mehmet Aslanoglu et al.
Chemical & pharmaceutical bulletin, 56(3), 282-286 (2008-03-04)
A reliable and reproducible method for the determination of uric acid in urine samples has been developed. The method is based on the modification of a glassy carbon electrode by 3-acetylthiophene using cyclic voltammetry. The poly(3-acetylthiophene) modified glassy carbon electrode

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