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170925

4-Nitrobenzenesulfonyl chloride

Name: 4-Nitrobenzenesulfonyl chloride
Brand: ALDRICH

technical grade, 90%

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About This Item

Linear Formula:

O₂NC₆H₄SO₂Cl

CAS Number:

98-74-8

Molecular Weight:

221.62

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24850336

EC Number:

202-697-9

Beilstein/REAXYS Number:

746543

MDL number:

MFCD00007445

Assay:

90%

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Properties

grade

technical grade

Quality Level

100

assay

90%

mp

66-70 °C (lit.)

SMILES string

[O-][N+](=O)c1ccc(cc1)S(Cl)(=O)=O

InChI

1S/C6H4ClNO4S/c7-13(11,12)6-3-1-5(2-4-6)8(9)10/h1-4H

InChI key

JXRGUPLJCCDGKG-UHFFFAOYSA-N

Description

Application

4-Nitrobenzenesulfonyl chloride was used in the synthesis of [Cu(bipy)2Cl](nbs) where bipy = 2,2′-bipyridine, nbs = 4-nitrobenzenesulfonate. It was also used to determine estrogens in biological fluids.

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pictograms

GHS08,GHS05,GHS07

signalword

Danger

hcodes

H317,H318,H361f

pcodes

P202 - P261 - P280 - P302 + P352 - P305 + P351 + P338 - P308 + P313

Hazard Classifications

Eye Dam. 1 - Repr. 2 - Skin Sens. 1A

Storage Class

11 - Combustible Solids

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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Procedure for increasing the detection responses of estrogens in LC-MS based on introduction of a nitrobenzene moiety followed by electron capture atmospheric pressure chemical ionization.

Tatsuya Higashi et al.

Analytical and bioanalytical chemistry, 386(3), 658-665 (2006-04-13)

A practical procedure for determining estrogens in biological fluids has been studied using liquid chromatography-electron capture atmospheric pressure chemical ionization-mass spectrometry combined with derivatization. Among the commercially available reagents (4-nitrobenzoyl chloride, 2,4-dinitrofluorobenzene, 4-nitrobenzenesulfonyl chloride and 4-nitrobenzyl bromide), 4-nitrobenzenesulfonyl chloride was

Synthesis and Crystal Structure of a Five-Coordinate Complex of Copper(II) with 4-Nitrobenzenesulfonate and 2, 2'-Bipyridine.

Mahboubeh A Sharif et al.

Acta chimica Slovenica, 59(2), 289-293 (2012-06-01)

[Cu(bipy)2Cl](nbs) (1) (bipy = 2,2'-bipyridine, nbs = 4-nitrobenzenesulfonate) was obtained from the reaction of 4-nitrobenzenesulfonyl chloride and 2-amine-4-methylopyridine with CuCl2 in the presence of 2,2'-bipyridine and characterized by elemental analysis, IR spectra and X-ray single-crystal diffraction. The asymmetric unit of

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
170925-25G	04061832418735