2,3,4,5,6-Pentafluoroaniline
2,3,4,5,6-Pentafluoroaniline structure
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Common Name | 2,3,4,5,6-Pentafluoroaniline | ||
|---|---|---|---|---|
| CAS Number | 771-60-8 | Molecular Weight | 183.079 | |
| Density | 1.6±0.1 g/cm3 | Boiling Point | 156.4±35.0 °C at 760 mmHg | |
| Molecular Formula | C6H2F5N | Melting Point | 33-35 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 73.9±0.0 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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The pH-dependence of organofluorine binding domain preference in dissolved humic acid.
Chemosphere 90(2) , 270-5, (2013) In this study we explore the relationship between solution pH and the distribution of the binding interactions at different domains of a dissolved humic acid (HA) for three xenobiotics: pentafluoroaniline (PFA), pentafluorophenol (PFP), and hexafluorobenzene ... |
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Molecular rearrangement reactions in the gas phase triggered by electron attachment.
Phys. Chem. Chem. Phys. 15(13) , 4754-66, (2013) Bond formation and rearrangement reactions in gas phase electron attachment were studied through dissociative electron attachment (DEA) to pentafluorotoluene (PFT), pentafluoroaniline (PFA) and pentafluorophenol (PFP) in the energy range 0-14 eV. In the case ... |
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Bioactivation of 4-fluorinated anilines to benzoquinoneimines as primary reaction products.
Chem. Biol. Interact. 77(3) , 263-81, (1991) Metabolism and bioactivation of fluoroanilines was studied both in vitro in microsomal systems and in vivo. 4-Fluoroaniline and pentafluoroaniline and their non-para fluorinated analogues were used as the model compounds. Special attention was focussed on bio... |
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Action of new organometallic complexes against Leishmania donovani.
J. Antimicrob. Chemother. 40(1) , 47-57, (1997) The action of 16 newly synthesized metal complexes having the general structure cis-Pt-(II)-Xn-Ln have been tested in vitro against the promastigote forms of Leishmania donovani. The metal complexes at 24 h and maximum dosages inhibited growth from 0%, e.g. i... |
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Pentafluorophenylammonium triflate (PFPAT): an efficient, practical, and cost-effective catalyst for esterification, thioesterification, transesterification, and macrolactone formation. Funatomi T, et al.
Green Chem. 8(12) , 1022-1027, (2006)
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Bis (salicylaldiminato) titanium complexes containing bulky imine substituents: Synthesis, characterization and ethene polymerization studies. Parssinen A, et al.
Eur. J. Inorg. Chem. 2005(11) , 2100-2109, (2005)
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