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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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Related Categories

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

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Certificates of Analysis (COA)

Lot/Batch Number
BCCC4624
BCBR0461V
BCBL7774V
BCBJ3311V
BCBJ0656V

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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
Tetrahedron, 63, 8164-8164 (2007)
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

SKUGTIN
272248-10G
272248-100G4061838348333
272248-10KG
272248-25G4061826144077
272248-5G4061826144084

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