N27209
4-Nitrothiophenol
technical grade, 80%
Synonym(s):
p-Nitrophenyl mercaptan, pNTP, 4-Nitrobenzenethiol
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About This Item
Linear Formula:
O2NC6H4SH
CAS Number:
Molecular Weight:
155.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-436-4
Beilstein/REAXYS Number:
606924
MDL number:
Assay:
80%
Form:
solid
Product Name
4-Nitrothiophenol, technical grade, 80%
InChI key
AXBVSRMHOPMXBA-UHFFFAOYSA-N
InChI
1S/C6H5NO2S/c8-7(9)5-1-3-6(10)4-2-5/h1-4,10H
SMILES string
[O-][N+](=O)c1ccc(S)cc1
grade
technical grade
assay
80%
form
solid
mp
72-77 °C (lit.)
storage temp.
2-8°C
Quality Level
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Application
4-Nitrothiophenol has been used in the synthesis of dual emission fluorescent probe for the differential sensing of of glutathione (GSH) and cysteine/homocysteine (Cys/Hcy). pNTP can also be used to synthesize diaryl thioethers via copper-catalyzed C-S coupling reaction.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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B O Skadtchenko et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 57A(5), 1009-1016 (2001-05-26)
The interpretation of the surface-enhanced Raman scattering (SERS) spectra of p-nitrothiophenol (p-NTP) is reported. SERS spectra were obtained by vacuum evaporation and casting of p-NTP onto silver island films, and also from colloidal silver solutions. The vibrational spectra of the
Qiaofeng Yao et al.
Nature communications, 8(1), 1555-1555 (2017-11-18)
Precise control of alloying sites has long been a challenging pursuit, yet little has been achieved for the atomic-level manipulation of metallic nanomaterials. Here we describe utilization of a surface motif exchange (SME) reaction to selectively replace the surface motifs
Ze-Yuan Dong et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 12(13), 3575-3579 (2006-02-24)
To elucidate the relationships between molecular recognition and catalytic ability, we chose three assay systems using three different thiol substrates, glutathione (GSH), 3-carboxyl-4-nitrobenzenethiol (CNBSH), and 4-nitrobenzenethiol (NBSH), to investigate the glutathione peroxidase (GPx) activities of 2,2'-ditellurobis(2-deoxy-beta-cyclodextrin) (2-TeCD) in the presence
Z G Dai et al.
Nanotechnology, 23(33), 335701-335701 (2012-07-31)
Control of the plasmon-driven chemical reaction for the transformation of 4-nitrobenzenethiol to p,p'-dimercaptoazobenzene by Ag nanoparticle arrays was studied. The Ag nanoparticle arrays were fabricated by means of nanosphere lithography. By changing the PS particle size, the localized surface plasmon
Ligand-free copper-catalyzed C? S coupling of aryl iodides and thiols.
Sperotto E, et al.
The Journal of Organic Chemistry, 73(14), 5625-5628 (2008)
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