Skip to Content
Merck
All Photos(2)

Documents

108669

Sigma-Aldrich

4-Bromobenzenesulfonyl chloride

98%

Synonym(s):

p-Bromobenzenesulfonyl chloride, Brosyl chloride

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
BrC6H4SO2Cl
CAS Number:
98-58-8
Molecular Weight:
255.52
Beilstein:
743518
EC Number:
202-683-2
MDL number:
MFCD00007437
UNSPSC Code:
12352100
PubChem Substance ID:
24846817
NACRES:
NA.22

Quality Level

100

Assay

98%

bp

153 °C/15 mmHg (lit.)

mp

73-75 °C (lit.)

SMILES string

ClS(=O)(=O)c1ccc(Br)cc1

InChI

1S/C6H4BrClO2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H

InChI key

KMMHZIBWCXYAAH-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

4-Bromobenzenesulfonyl chloride was used as activating agent in the synthesis of oligodeoxyribo- and oligoribo- nucleotides in solution. It was used in the synthesis of 4-(N-allylsulfamoyl)phenylboronic acid.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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

Xiaobao Li et al.
Analytical biochemistry, 372(2), 227-236 (2007-10-20)
Two new types of boronate affinity solid phases were synthesized and characterized. The materials were prepared by silylation of porous silica gel with monochlorosilane derivatives containing synthetic sulfonyl- and sulfonamide-substituted phenylboronic acids. The new solid phases were evaluated for boronate
Phosphotriester approach to the synthesis of oligonucleotides: a reappraisal.
Reese CB and Pei-Zhuo Z.
Journal of the Chemical Society. Perkin Transactions 1, 1(19), 2291-2301 (1993)
Tsurng-Juhn Huang et al.
European journal of medicinal chemistry, 90, 428-435 (2014-12-03)
Hepatitis B virus (HBV) is a causative reagent that frequently causes progressive liver diseases, leading to the development of acute, chronic hepatitis, cirrhosis, and eventually hepatocellular carcinoma (HCC). Despite several antiviral drugs including interferon-α and nucleotide derivatives are approved for

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