Date published: 2025-10-16

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3-Nitrobenzonitrile (CAS 619-24-9)

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Alternate Names:
3-Cyanonitrobenzene
CAS Number:
619-24-9
Molecular Weight:
148.12
Molecular Formula:
C7H4N2O2
Supplemental Information:
This is as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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3-Nitrobenzonitrile has been used in the synthesis of a diverse array of heterocyclic compounds, including derivatives like pyridine, indole, and quinoline. In vitro, it has exhibited toxicity towards human cells and has demonstrated the ability to trigger apoptosis in human cancer cells. Additionally, 3-Nitrobenzonitrilenitrile has proven to inhibit the activity of enzymes cytochrome P450 and aldehyde oxidase.


3-Nitrobenzonitrile (CAS 619-24-9) References

  1. Use of 3-nitrobenzonitrile as an additive for improved sensitivity in sonic-spray ionization mass spectrometry.  |  Kanaki, K. and Pergantis, SA. 2014. Rapid Commun Mass Spectrom. 28: 2661-9. PMID: 25366412
  2. Improving the Sensitivity of Matrix-Assisted Ionization (MAI) Mass Spectrometry Using Ammonium Salts.  |  Chubatyi, ND. and McEwen, CN. 2015. J Am Soc Mass Spectrom. 26: 1649-56. PMID: 26122522
  3. A dopant for improved sensitivity in easy ambient sonic-spray ionization mass spectrometry.  |  Santos, JM., et al. 2016. J Mass Spectrom. 51: 53-61. PMID: 26757072
  4. Ambient Profiling of Phenolic Content in Tea Infusions by Matrix-Assisted Ionization in Vacuum.  |  Cody, RB. 2018. J Am Soc Mass Spectrom. 29: 1594-1600. PMID: 29845560
  5. Ion formation in droplet-assisted ionization.  |  Apsokardu, MJ., et al. 2021. Rapid Commun Mass Spectrom. 35 Suppl 1: e8227. PMID: 29971846
  6. Electron-withdrawing effects on the molecular structure of 2- and 3-nitrobenzonitrile revealed by broadband rotational spectroscopy and their comparison with 4-nitrobenzonitrile.  |  Graneek, JB., et al. 2018. Phys Chem Chem Phys. 20: 22210-22217. PMID: 30118134
  7. Mechanochemical Catalytic Transfer Hydrogenation of Aromatic Nitro Derivatives.  |  Portada, T., et al. 2018. Molecules. 23: PMID: 30513686
  8. Toward understanding the ionization mechanism of matrix-assisted ionization using mass spectrometry experiment and theory.  |  Lee, C., et al. 2021. Rapid Commun Mass Spectrom. 35 Suppl 1: e8382. PMID: 30623523
  9. Matrix-assisted ionization mass spectrometry in targeted protein analysis - An initial evaluation.  |  Skjaervø, Ø., et al. 2021. Rapid Commun Mass Spectrom. 35 Suppl 1: e8437. PMID: 30883961
  10. New mass spectrometry concepts for characterization of synthetic polymers and additives.  |  Inutan, ED., et al. 2020. Rapid Commun Mass Spectrom. 34 Suppl 2: e8768. PMID: 32107802
  11. Method for Molecular Layer Deposition Using Gas Cluster Ion Beam Sputtering with Example Application In Situ Matrix-Enhanced Secondary Ion Mass Spectrometry.  |  Lorenz, M., et al. 2021. Anal Chem. 93: 3436-3444. PMID: 33571411
  12. Organocatalytic Reduction of Aromatic Nitro Compounds: The Use of Solid-Supported Phenyl(2-quinolyl)methanol.  |  Giomi, D., et al. 2022. ACS Omega. 7: 35170-35179. PMID: 36211086
  13. Synthesis and Antibiotic Activity of Chitosan-Based Comb-like Co-Polypeptides.  |  Enright, TP., et al. 2023. Mar Drugs. 21: PMID: 37103382

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

3-Nitrobenzonitrile, 25 g

sc-231879
25 g
$65.00