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Key Documents

N21022

Sigma-Aldrich

4-Nitrophenyl disulfide

Synonym(s):

p,p′-Dinitrodiphenyl disulfide, Bis(4-nitrophenyl) disulfide, Bis(p-nitrophenyl) disulfide, NSC 4566, NSC 677446

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About This Item

Linear Formula:
(O2NC6H4)2S2
CAS Number:
Molecular Weight:
308.33
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

form

powder

SMILES string

[O-][N+](=O)c1ccc(SSc2ccc(cc2)[N+]([O-])=O)cc1

InChI

1S/C12H8N2O4S2/c15-13(16)9-1-5-11(6-2-9)19-20-12-7-3-10(4-8-12)14(17)18/h1-8H

InChI key

KWGZRLZJBLEVFZ-UHFFFAOYSA-N

Application

Reactant or reagent involved in:
  • Electrophilic cyclization of 2-alkynylanisoles or alkynylanilines
  • Oxidative chlorination to sulfonyl chlorides
  • Arylation with triarylbismuthanes
  • Decarboxylative cross-coupling with dialkoxybenzoic acids
  • Disulfidation of alkenes

Pictograms

Health hazardExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2

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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Use of p-nitrophenyl disulfide to measure reductive capacity of intact cells.
C Gitler et al.
Methods in enzymology, 251, 279-286 (1995-01-01)
Homan Kang et al.
Scientific reports, 5, 10144-10144 (2015-05-29)
Recently, preparation and screening of compound libraries remain one of the most challenging tasks in drug discovery, biomarker detection, and biomolecular profiling processes. So far, several distinct encoding/decoding methods such as chemical encoding, graphical encoding, and optical encoding have been

Articles

While Markovnikov alkene reactivity is very well developed and utilized commonly in the synthesis of commodity and research chemicals, catalytic access to the anti-Markovnikov-selective adducts is a much less-developed endeavor.

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