Date published: 2025-10-19

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3,5-Dimethylpyrazole (CAS 67-51-6)

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Application:
3,5-Dimethylpyrazole is common pyrazolato ligand
CAS Number:
67-51-6
Molecular Weight:
96.13
Molecular Formula:
C5H8N2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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3,5-Dimethylpyrazole (3,5-DMP) is a versatile organic compound widely employed in organic chemistry for the synthesis of diverse compounds. It plays a role as a significant reagent in organic synthesis. 3,5-Dimethylpyrazole has been utilized in the production of a variety of other compounds, including polymers, surfactants, and catalysts. Its catalytic properties enable the activation of reactants, resulting in enhanced reaction rates. Furthermore, 3,5-Dimethylpyrazole serves as a ligand in metal-catalyzed reactions, facilitating the formation of intricate and complex molecules.


3,5-Dimethylpyrazole (CAS 67-51-6) References

  1. Vibrational spectra of 3,5-dimethylpyrazole and deuterated derivatives.  |  Orza, JM., et al. 2000. Spectrochim Acta A Mol Biomol Spectrosc. 56A: 1469-98. PMID: 10907878
  2. Solvent induced reactivity of 3,5-dimethylpyrazole towards zinc (II) carboxylates.  |  Sarma, R., et al. 2009. Dalton Trans. 7428-36. PMID: 19727464
  3. Experimental FTIR, FT-IR (gas phase), FT-Raman and NMR spectra, hyperpolarizability studies and DFT calculations of 3,5-dimethylpyrazole.  |  Sundaraganesan, N., et al. 2009. Spectrochim Acta A Mol Biomol Spectrosc. 74: 788-97. PMID: 19729338
  4. H/D isotopic and temperature effects in the polarized IR spectra of hydrogen-bond cyclic trimers in the crystal lattices of acetone oxime and 3,5-dimethylpyrazole.  |  Flakus, HT., et al. 2012. J Phys Chem A. 116: 11553-67. PMID: 23106525
  5. Spectroscopic studies and molecular orbital calculations of charge transfer complexation between 3,5-dimethylpyrazole with DDQ in acetonitrile.  |  Habeeb, MM., et al. 2015. Spectrochim Acta A Mol Biomol Spectrosc. 142: 196-203. PMID: 25703364
  6. Determination of 3,5 - dimethylpyrazolium glyceroborate nitrification inhibitor in nitrogen fertilizer samples: HPLC-DAD method development and validation for 3,5 - dimethylpyrazole.  |  Şahan, S., et al. 2017. J Chromatogr B Analyt Technol Biomed Life Sci. 1068-1069: 277-281. PMID: 29132907
  7. Synthesis and bioactivity of 3,5-dimethylpyrazole derivatives as potential PDE4 inhibitors.  |  Hu, DK., et al. 2018. Bioorg Med Chem Lett. 28: 3276-3280. PMID: 30131240
  8. Antitubercular 2-Pyrazolylpyrimidinones: Structure-Activity Relationship and Mode-of-Action Studies.  |  Soares de Melo, C., et al. 2021. J Med Chem. 64: 719-740. PMID: 33395287
  9. In Situ Grignard Metalation Method for the Synthesis of Hauser Bases.  |  Sengupta, S., et al. 2022. Chemistry. 28: e202201359. PMID: 35686618
  10. Mimicking the Cu Active Site of Lytic Polysaccharide Monooxygenase Using Monoanionic Tridentate N-Donor Ligands.  |  Bouchey, CJ., et al. 2022. ACS Omega. 7: 35217-35232. PMID: 36211076
  11. Synthesis, Structure and Molecular Docking of New 4,5-Dihydrothiazole Derivatives Based on 3,5-Dimethylpyrazole and Cytisine and Salsoline Alkaloids.  |  Ibrayev, MK., et al. 2022. Molecules. 27: PMID: 36364423
  12. Reactive Disperse Dyes Bearing Various Blocked Isocyanate Groups for Digital Textile Printing Ink.  |  Jeong, S., et al. 2023. Molecules. 28: PMID: 37175223
  13. Allylic oxidation with 3, 5-dimethylpyrazole. Chromium trioxide complex steroidal. DELTA. 5-7-ketones.  |  Salmond, W. G., Barta, M. A., & Havens, J. L. 1978. The Journal of Organic Chemistry. 43(10): 2057-2059.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

3,5-Dimethylpyrazole, 100 g

sc-238701
100 g
$143.00