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272248

Sigma-Aldrich

4-Nitrobenzenesulfonyl chloride

97%

Synonym(s):

4-Nitrobenzene-1-sulfonyl chloride, 4-Nitrobenzenesulfonic acid chloride, 4-Nitrobenzenesulfonyl chloride, 4-Nitrophenyl-1-sulfonyl chloride, 4-Nitrophenylsulfonyl chloride, Nosyl chloride, p-Nitrobenzenesulfonyl chloride, p-Nitrophenylsulfonyl chloride, p-Nosyl chloride

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About This Item

Linear Formula:
O2NC6H4SO2Cl
CAS Number:
98-74-8
Molecular Weight:
221.62
Beilstein:
746543
EC Number:
202-697-9
MDL number:
MFCD00007445
UNSPSC Code:
12352100
PubChem Substance ID:
24856461
NACRES:
NA.22

Quality Level

200

Assay

97%

mp

66-70 °C (lit.)

functional group

nitro

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

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Application

4-Nitrobenzenesulfonyl chloride was used in the synthesis of
  • [Cu(bipy)2Cl](nbs) (1) (bipy = 2,2′-bipyridine, nbs = 4-nitrobenzenesulfonate)
  • hydroxylamines of sulfadiazine and sulfamethoxazole
  • solution phase peptide using N-nosyl-α-amino acids.

Signal Word

Danger

Hazard Statements

H317,H318,H361f

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

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’.

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Tetrahedron, 63, 8164-8164 (2007)
Jason Jones et al.
Analytical chemistry, 92(4), 3483-3491 (2020-01-29)
For decades, there has been immense progress in miniaturizing analytical methods based on electrophoresis to improve sensitivity and to reduce sample volumes, separation times, and/or equipment cost and space requirements, in applications ranging from analysis of biological samples to environmental
Balázs Pásztói et al.
Polymers, 12(11) (2020-11-01)
Endfunctional polymers possess significant industrial and scientific importance. Sulfonyl endgroups, such as tosyl and nosyl endfunctionalities, due their ease of substitution are highly desired for a variety of polymer structures. The sulfonylation of hydroxyl-terminated polyisobutylene (PIB-OH), a chemically and thermally
M J Rieder et al.
The Journal of pharmacology and experimental therapeutics, 244(2), 724-728 (1988-02-01)
Among the most serious side effects of sulfonamides are hypersensitivity reactions, the pathogenesis of which has been suggested to be mediated by reactive metabolites. We have previously demonstrated dose-related covalent binding and toxicity of reactive intermediates of sulfonamides generated by
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
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