Skip to Content
Merck
All Photos(1)

Documents

478598

Sigma-Aldrich

2-Chlorobenzenesulfonyl isocyanate

90%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
ClC6H4SO2NCO
CAS Number:
Molecular Weight:
217.63
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

Assay

90%

impurities

10% 2-chlorobenzenesulfonyl chloride

refractive index

n20/D 1.559 (lit.)

bp

285 °C (lit.)

density

1.484 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

Clc1ccccc1S(=O)(=O)N=C=O

InChI

1S/C7H4ClNO3S/c8-6-3-1-2-4-7(6)13(11,12)9-5-10/h1-4H

InChI key

LALCDSDHLXWTTL-UHFFFAOYSA-N

General description

2-Chlorobenzenesulfonyl isocyanate is an aryl isocyanate that can be synthesized by the catalytic carbonylation of potassium N,2- dichlorobenzenesulfonamidate in acetonitrile. The C-acylation of nitrogen bearing heterocycles using 2-chlorobenzenesulfonyl isocyanate has been reported.

Application

2-Chlorobenzenesulfonyl isocyanate may be used in the synthesis of N-thiazolyl-N′-(2-chlorobenzenesulfonyl)urea derivatives and N-(2-chlorophenylsulfonyl)-N′-(4-methoxy-6-methyl-triazin-2-yl)urea.

Pictograms

Health hazardCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Resp. Sens. 1 - Skin Corr. 1B - Skin Sens. 1

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

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

Thiazolecarboxylic acid derivatives. 1. N-substituted 2-amino-4-methylthiazole-5-carboxylic acid derivatives.
Dovlatyan VV, et al.
Chemistry of Heterocyclic Compounds, 40(1), 84-89 (2004)
C-Acylation of Electron-Rich Heterocycles by o-Chlorobenzenesulfonyl Isocyanate.
Nam NL, et al.
ChemInform, 27(35) (1996)
Catalytic carbonylation of potassium N,2-dichlorobenzenesulfonamidate to sulfonyl isocyanate.
Besenyei G, et al.
Reaction Kinetics and Catalysis Letters, 62(2), 321-326 (1997)

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