2-Trifluoromethylphenylhydrazine
2-Trifluoromethylphenylhydrazine structure
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Common Name | 2-Trifluoromethylphenylhydrazine | ||
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| CAS Number | 365-34-4 | Molecular Weight | 176.139 | |
| Density | 1.4±0.1 g/cm3 | Boiling Point | 221.5±40.0 °C at 760 mmHg | |
| Molecular Formula | C7H7F3N2 | Melting Point | 55-58°C | |
| MSDS | Chinese USA | Flash Point | 87.7±27.3 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Eur. J. Med. Chem. 28 , 185, (1993)
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Reactivity of (E)-4-Hydroxy-2-nonenal with Fluorinated Phenylhydrazines: Towards the Efficient Derivatization of an Elusive Key Biomarker of Lipid Peroxidation. Matera R, et al.
European J. Org. Chem. 20 , 3841-51, (2012)
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Nonpeptide angiotensin II antagonists derived from 1H-pyrazole-5-carboxylates and 4-aryl-1H-imidazole-5-carboxylates.
J. Med. Chem. 36 , 3595, (1993) Two series of potential angiotensin II antagonists derived from carboxyl-functionalized "diazole" heterocycles have been prepared and evaluated. Initially, a limited investigation of 4-arylimidazole-5-carboxylates led to 2-n-butyl-4-(2-chlorophenyl)-1-[[2'-(1... |
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Triazolinone biphenylsulfonamide derivatives as orally active angiotensin II antagonists with potent AT1 receptor affinity and enhanced AT2 affinity.
J. Med. Chem. 37 , 2808, (1994) Several series of 2,4-dihydro-2,4,5-trisubstituted-3H-1,2,4-triazol-3-ones with acidic sulfonamide replacements of tetrazole at the 2'-position of the biphenyl-4-ylmethyl side chain at N4 were prepared and tested as angiotensin II (AII) antagonists. Preferred... |