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108669

4-Bromobenzenesulfonyl chloride

Name: 4-Bromobenzenesulfonyl chloride
Brand: ALDRICH

98%

Synonym(s):

p-Bromobenzenesulfonyl chloride, Brosyl chloride

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About This Item

Linear Formula:

BrC₆H₄SO₂Cl

CAS Number:

98-58-8

Molecular Weight:

255.52

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24846817

EC Number:

202-683-2

Beilstein/REAXYS Number:

743518

MDL number:

MFCD00007437

Assay:

98%

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Properties

Quality Level

100

assay

98%

bp

153 °C/15 mmHg (lit.)

mp

73-75 °C (lit.)

functional group

bromo

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

Description

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

GHS05

signalword

Danger

hcodes

H314

pcodes

P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

危险化学品

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Synthesis of sulfonamide- and sulfonyl-phenylboronic acid-modified silica phases for boronate affinity chromatography at physiological pH.

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)

Design, synthesis, and bioevaluation of paeonol derivatives as potential anti-HBV agents.

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

Global Trade Item Number

SKU	GTIN
108669-25G	04061838686275
108669-100G	04061838344816