| Weight | 96.133 g/mol |
|---|---|
| Formula | C5H8N2 |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
3,5-Dimethylpyrazole (67-51-6)
3,5-dimethylpyrazole, sodium salt
Score:
#6363 in Chemistry
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- Allylic oxidation with 3,5-dimethylpyrazole. Chromium trioxide complex steroidal .DELTA.5-7-ketones (Journal of Organic Chemistry, 1978)
- Intermolecular triple proton and deuteron transfer in crystalline 3,5-dimethylpyrazole studied by NMR, NQR and X-ray methods (Journal of the American Chemical Society, 1989)
- Chromium trioxide-3, 5-dimethylpyrazole complex as a reagent for oxidation of alcohols to carbonyl compounds (Tetrahedron Letters, 1973)
- REACTION OF DIOXYGEN WITH [CU(DMPZ)]N (HDMPZ = 3,5-DIMETHYLPYRAZOLE) - CRYSTAL-STRUCTURE, REACTIVITY, AND CATALYTIC PROPERTIES OF [CU8(DMPZ)8(OH)8] (Inorganic Chemistry, 1991)
- Dynamic intermolecular tautomerism of 3,5-dimethylpyrazole in the solid state by carbon-13 CP/MAS NMR spectroscopy and x-ray crystallography (Journal of the American Chemical Society, 1985)
- Experimental FTIR, FT-IR (gas phase), FT-Raman and NMR spectra, hyperpolarizability studies and DFT calculations of 3,5-dimethylpyrazole. (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2009)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3,5-dimethylpyrazole, sodium salt
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SMILESCC1=CC(=NN1)C
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InChIKeySDXAWLJRERMRKF-UHFFFAOYSA-N
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