Molecular structure of 4-Nitrothiophenol, CAS Number: 1849-36-1
4-Nitrothiophenol (CAS 1849-36-1)
CAS Number:
1849-36-1
Purity:
≥95%
Molecular Weight:
155.17
Molecular Formula:
C6H5NO2S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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4-Nitrothiophenol finds utility as a reagent for synthesizing a wide range of organic compounds, serving as a vital intermediate in the production of dyes and other organic substances. Its significance extends to the synthesis of thiophene-based compounds. Furthermore, 4-Nitrothiophenol exhibits catalytic properties and has been instrumental in the synthesis of diverse heterocyclic compounds.
4-Nitrothiophenol (CAS 1849-36-1) References
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- The importance of plasmonic heating for the plasmon-driven photodimerization of 4-nitrothiophenol. | Sarhan, RM., et al. 2019. Sci Rep. 9: 3060. PMID: 30816134
- Role of Valence Band States and Plasmonic Enhancement in Electron-Transfer-Induced Transformation of Nitrothiophenol. | Schürmann, R., et al. 2019. J Phys Chem Lett. 10: 3153-3158. PMID: 31117676
- A composite prepared from gold nanoparticles and a metal organic framework (type MOF-74) for determination of 4-nitrothiophenol by surface-enhanced Raman spectroscopy. | Zhang, Y., et al. 2019. Mikrochim Acta. 186: 477. PMID: 31250191
- Bifunctional Metal Nanocrystals for Catalyzing and Reporting on Chemical Reactions. | Shi, S. and Qin, D. 2020. Angew Chem Int Ed Engl. 59: 3782-3792. PMID: 31529749
- Kinetic and Mechanistic Investigation of the Photocatalyzed Surface Reduction of 4-Nitrothiophenol Observed on a Silver Plasmonic Film via Surface-Enhanced Raman Scattering. | Qiu, L., et al. 2020. ACS Appl Mater Interfaces. 12: 21133-21142. PMID: 32286058
- Interaction of 4-nitrothiophenol with low energy electrons: Implications for plasmon mediated reactions. | Schürmann, R., et al. 2020. J Chem Phys. 153: 104303. PMID: 32933272
- The Effect of Surface Modification of Gold Nanotriangles for Surface-Enhanced Raman Scattering Performance. | Koetz, J. 2020. Nanomaterials (Basel). 10: PMID: 33147806
- Decoding the kinetic limitations of plasmon catalysis: the case of 4-nitrothiophenol dimerization. | Koopman, W., et al. 2020. Nanoscale. 12: 24411-24418. PMID: 33300518
- Au-on-Ag nanostructure forin-situSERS monitoring of catalytic reactions. | He, S., et al. 2022. Nanotechnology. 33: PMID: 34983032
- Development of Mild Chemical Catalysis Conditions for m1A-to-m6A Rearrangement on RNA. | Liu, H., et al. 2022. ACS Chem Biol. 17: 1334-1342. PMID: 35593877
- Quantifying Hot Electron Energy Contributions in Plasmonic Photocatalysis Using Electrochemical Surface-Enhanced Raman Spectroscopy. | Yu, L., et al. 2022. J Phys Chem Lett. 13: 5495-5500. PMID: 35695751
- Hydrophobic plasmonic silver membrane as SERS-active catcher for rapid and ultrasensitive Cu(II) detection. | He, L., et al. 2022. J Hazard Mater. 440: 129731. PMID: 35963095
- Collective Mid-Infrared Vibrations in Surface-Enhanced Raman Scattering. | Mueller, NS., et al. 2022. Nano Lett. 22: 7254-7260. PMID: 36037474
- HPLC determination of N-nitrosomethylurea in biological fluids by reaction with 4-nitrothiophenol. | Yamamoto, M., et al. 1986. Food Chem Toxicol. 24: 247-50. PMID: 3957178
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
4-Nitrothiophenol, 5 g | sc-232931 | 5 g | $96.00 |