1-Aminopyridinium iodide
September 8, 2021
3-Amino-5-methylisoxazole
September 8, 2021
3-Methyl-5-(trifluoromethyl)-1H-pyrazole
3-Methyl-5-(trifluoromethyl)pyrazole is a pyrazole derivative. It has been reported to be synthesized from 3-methyl-5-trifluoromethyl-1H-pyrazole.
| Product | 3-Methyl-5-(trifluoromethyl)-1H-pyrazole | ||
| CAS No. | 10010-93-2 | ||
| Synonyms | TIMTEC-BB SBB004075;
1H-Pyrazole,3-methyl-5-(trifluoromethyl)-; CBI-BB ZERO/006128; BUTTPARK 29\08-72; BUTTPARK 76\07-66; ART-CHEM-BB B014453; 3-TRIFLUOROMETHYL-5-(METHYL)PYRAZOLE. |
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| SMILES | CC1=CC(=NN1)C(F)(F)F | ||
| InChI | 1S/C5H5F3N2/c1-3-2-4(10-9-3)5(6,7)8/h2H,1H3,(H,9,10) | ||
| InChI key | DLCHCAYDSKIFIN-UHFFFAOYSA-N | ||
| Availability | In Stock | ||
| MF. | C5H5F3N2 | MW. | 150.1 |
| Melting Point | 88-90 °C | Boiling Point | 187℃ |
| Appearance | White powder | Purity | 95% |
| Application |
For research use only |
Storage | RT |
| COA & NMR | Download | MSDS | Download |
Reference
[1] Synthesis and Structure of Pyrazole-Containing Ferrocenyl Ligands for Asymmetric Catalysis.Burckhardt U, et al.Organometallics, 14(11), 5415-5425 (1995)
[2] Reaction of β-alkoxyvinyl halomethyl ketones with cyanoacetohydrazide.Martins MAP, et al. Journal of the Brazilian Chemical Society, 19(7), 1361-1368 (2008)
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