Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

288985

Sigma-Aldrich

2-Thiophenecarbonyl chloride

97%

Synonym(s):

α-Thenoyl chloride

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C5H3ClOS
CAS Number:
5271-67-0
Molecular Weight:
146.59
Beilstein/REAXYS Number:
110145
EC Number:
226-092-4
MDL number:
MFCD00005428
UNSPSC Code:
12352100
PubChem Substance ID:
24857375
NACRES:
NA.22

assay

97%

form

liquid

refractive index

n20/D 1.590 (lit.)

bp

206-208 °C (lit.)

density

1.371 g/mL at 25 °C (lit.)

functional group

acyl chloride

storage temp.

2-8°C

SMILES string

ClC(=O)c1cccs1

InChI

1S/C5H3ClOS/c6-5(7)4-2-1-3-8-4/h1-3H

InChI key

QIQITDHWZYEEPA-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

The postfunctionalization reaction of 2-thiophenecarbonyl chloride with single walled carbon nanotubes (SWCNTs) was studied.

Application

2-Thiophenecarbonyl chloride was used in the synthesis of building blocks derived from ornithine by undergoing acylation/sulphonation of copper complex of orthinine.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H290,H314

Hazard Classifications

Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

194.0 °F

flash_point_c

90 °C

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
STBK8877
STBK5601
STBJ4637
STBH9211
STBG8199

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Ferdinand Hof et al.
Journal of the American Chemical Society, 135(49), 18385-18395 (2013-11-22)
The reactivity of reduced single walled carbon nanotubes (SWCNTs) (carbon nanotubides), prepared under strict inert conditions in a glovebox with respect to the covalent functionalization with hexyl iodide and subsequent exposure to ambient conditions (air, moisture), was systematically investigated by
T Lescrinier et al.
The journal of peptide research : official journal of the American Peptide Society, 49(2), 183-189 (1997-02-01)
Recently great interest has arisen in the synthesis of combinatorial libraries, and this technology provides a significant partner to contemporary strategies in rational design and lead discovery. By simple combination of a given set of building blocks, high numbers of

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service