Skip to Content
Merck
CN
All Photos(1)

Documents

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:
110145
EC Number:
226-092-4
MDL number:
MFCD00005428
UNSPSC Code:
12352100
PubChem Substance ID:
24857375
NACRES:
NA.22

Quality Level

200

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.)

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

Related Categories

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

Signal Word

Danger

Hazard Statements

H290,H314

Hazard Classifications

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

WGK

WGK 3

Flash Point(F)

194.0 °F

Flash Point(C)

90 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

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