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About This Item
Linear Formula:
O2NC6H4SC6H5
CAS Number:
Molecular Weight:
231.27
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
![1-NITRO-3-[(4-NITROPHENYL)SULFONYL]BENZENE AldrichCPR](/deepweb/assets/sigmaaldrich/product/structures/677/586/8fe37419-256f-45d7-97a7-baf639d88ee0/640/8fe37419-256f-45d7-97a7-baf639d88ee0.png)
Assay
97%
form
solid
mp
52-55 °C (lit.)
SMILES string
[O-][N+](=O)c1ccc(Sc2ccccc2)cc1
InChI
1S/C12H9NO2S/c14-13(15)10-6-8-12(9-7-10)16-11-4-2-1-3-5-11/h1-9H
InChI key
RJCBYBQJVXVVKB-UHFFFAOYSA-N
General description
4-Nitrophenyl phenyl sulfide participates in copper-catalysed S-arylation of thiophenol derivatives with aryl halides.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
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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Mónica Carril et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 13(18), 5100-5105 (2007-03-28)
A novel protocol for the copper-catalysed S-arylation of thiophenol derivatives with aryl halides leading to diaryl sulfides is reported. The reactions were catalysed by a combination of a copper salt and a 1,2-diamine derivative (acting both as the ligand and
T R Juneja et al.
Mutation research, 263(1), 13-19 (1991-05-01)
4-Nitrodiphenyl thioether (4-NO2TE) and its various potential metabolites 4-nitroso- (4-NOTE), 4-hydroxylamino- (4-NHOHTE), 4-hydroxyacetylamino- [4-N(OH)ACTE], 4-acetoxy-acetylamino- [4-N(OAc)-ACTE], 4-amino- (4-ATE) and 4-acetamido- (4-AATE) were tested for their mutagenicity toward Salmonella typhimurium TA98 in the presence and absence of S9 activation system. 4-NO2TE
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